C3151071[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 330269	NM_000064.4(C3):c.4941G>A (p.Gln1647=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 330270	NM_000064.4(C3):c.4896C>T (p.Pro1632=)	C3	Single nucleotide variant (synonymous variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +3 more	GBenign
Select item 789661	NM_000064.4(C3):c.4878T>C (p.Thr1626=)	C3	Single nucleotide variant (synonymous variant)	not specified +6 more	GBenign/Likely benign
Select item 330271	NM_000064.4(C3):c.4855A>C (p.Ser1619Arg)	C3 (S1619R)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 330272	NM_000064.4(C3):c.4850+12C>A	C3	Single nucleotide variant (intron variant)	Complement component 3 deficiency +2 more	GConflicting classifications of pathogenicity
Select item 330273	NM_000064.4(C3):c.4827C>T (p.Ser1609=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 758206	NM_000064.4(C3):c.4824C>T (p.Ser1608=)	C3	Single nucleotide variant (synonymous variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 330274	NM_000064.4(C3):c.4803C>T (p.His1601=)	C3	Single nucleotide variant (synonymous variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 330275	NM_000064.4(C3):c.4767G>A (p.Lys1589=)	C3	Single nucleotide variant (synonymous variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 330276	NM_000064.4(C3):c.4759C>T (p.Pro1587Ser)	C3 (P1587S)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 732571	NM_000064.4(C3):c.4645C>T (p.Leu1549=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 330277	NM_000064.4(C3):c.4645C>A (p.Leu1549Met)	C3 (L1549M)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 330278	NM_000064.4(C3):c.4635C>T (p.Tyr1545=)	C3	Single nucleotide variant (synonymous variant)	Age related macular degeneration 9 +3 more	GBenign/Likely benign
Select item 330279	NM_000064.4(C3):c.4631-8C>T	C3	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 330280	NM_000064.4(C3):c.4631-9C>T	C3	Single nucleotide variant (intron variant)	not provided +4 more	GBenign/Likely benign
Select item 330281	NM_000064.4(C3):c.4535G>A (p.Arg1512His)	C3 (R1512H)	Single nucleotide variant (missense variant)	Age related macular degeneration 9 +3 more	GConflicting classifications of pathogenicity
Select item 893747	NM_000064.4(C3):c.4471C>T (p.Arg1491Trp)	C3 (R1491W)	Single nucleotide variant (missense variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 330282	NM_000064.4(C3):c.4457-4G>A	C3	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 330283	NM_000064.4(C3):c.4457-5C>T	C3	Single nucleotide variant (intron variant)	not provided +5 more	GBenign/Likely benign
Select item 892669	NM_000064.4(C3):c.4353C>G (p.Val1451=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 330284	NM_000064.4(C3):c.4319A>C (p.Asp1440Ala)	C3 (D1440A)	Single nucleotide variant (missense variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 330285	NM_000064.4(C3):c.4311C>T (p.Ala1437=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 893471	NM_000064.4(C3):c.4257G>A (p.Lys1419=)	C3	Single nucleotide variant (synonymous variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 633670	NM_000064.4(C3):c.4148C>A (p.Thr1383Asn)	C3 (T1383N)	Single nucleotide variant (missense variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 893472	NM_000064.4(C3):c.4121-4C>T	C3	Single nucleotide variant (intron variant)	Complement component 3 deficiency +2 more	GUncertain significance
Select item 330287	NM_000064.4(C3):c.4095C>G (p.Val1365=)	C3	Single nucleotide variant (synonymous variant)	Age related macular degeneration 9 +3 more	GConflicting classifications of pathogenicity
Select item 330288	NM_000064.4(C3):c.4030-4C>T	C3	Single nucleotide variant (intron variant)	Age related macular degeneration 9 +3 more	GConflicting classifications of pathogenicity
Select item 330289	NM_000064.4(C3):c.3993A>G (p.Thr1331=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 894695	NM_000064.4(C3):c.3970-15C>G	C3	Single nucleotide variant (intron variant)	Age related macular degeneration 9 +2 more	GUncertain significance
Select item 894696	NM_000064.4(C3):c.3953T>G (p.Leu1318Arg)	C3 (L1318R)	Single nucleotide variant (missense variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 892708	NM_000064.4(C3):c.3793G>A (p.Gly1265Ser)	C3 (G1265S)	Single nucleotide variant (missense variant)	Complement component 3 deficiency +2 more	GUncertain significance
Select item 330290	NM_000064.4(C3):c.3753C>A (p.Pro1251=)	C3	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign
Select item 330291	NM_000064.4(C3):c.3687C>T (p.Asn1229=)	C3	Single nucleotide variant (synonymous variant)	C3-related condition +4 more	GConflicting classifications of pathogenicity
Select item 330292	NM_000064.4(C3):c.3671G>A (p.Gly1224Asp)	C3 (G1224D)	Single nucleotide variant (missense variant)	C3-related condition +5 more	GConflicting classifications of pathogenicity
Select item 893502	NM_000064.4(C3):c.3586C>T (p.Leu1196=)	C3	Single nucleotide variant (synonymous variant)	Complement component 3 deficiency +2 more	GUncertain significance
Select item 893503	NM_000064.4(C3):c.3449C>G (p.Ser1150Trp)	C3 (S1150W)	Single nucleotide variant (missense variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +2 more	GUncertain significance
Select item 893806	NM_000064.4(C3):c.3411C>T (p.Asn1137=)	C3	Single nucleotide variant (synonymous variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +3 more	GConflicting classifications of pathogenicity
Select item 893807	NM_000064.4(C3):c.3407A>G (p.Asn1136Ser)	C3 (N1136S)	Single nucleotide variant (missense variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +3 more	GUncertain significance
Select item 894714	NM_000064.4(C3):c.3391-4T>C	C3	Single nucleotide variant (intron variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +3 more	GBenign
Select item 894715	NM_000064.4(C3):c.3391-6T>C	C3	Single nucleotide variant (intron variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +3 more	GBenign
Select item 892735	NM_000064.4(C3):c.3391-8T>C	C3	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 330293	NM_000064.4(C3):c.3299T>C (p.Leu1100Pro)	C3 (L1100P)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 330294	NM_000064.4(C3):c.3216G>T (p.Arg1072=)	C3	Single nucleotide variant (synonymous variant)	not specified +5 more	GBenign/Likely benign
Select item 892736	NM_000064.4(C3):c.3024G>A (p.Ser1008=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 330295	NM_000064.4(C3):c.2907C>T (p.Asp969=)	C3	Single nucleotide variant (synonymous variant)	Age related macular degeneration 9 +3 more	GConflicting classifications of pathogenicity
Select item 330296	NM_000064.4(C3):c.2901C>T (p.Leu967=)	C3	Single nucleotide variant (synonymous variant)	Age related macular degeneration 9 +4 more	GBenign/Likely benign
Select item 893831	NM_000064.4(C3):c.2863+15G>T	C3	Single nucleotide variant (intron variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +3 more	GConflicting classifications of pathogenicity
Select item 330297	NM_000064.4(C3):c.2863+7C>T	C3	Single nucleotide variant (intron variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +3 more	GBenign
Select item 389714	NM_000064.4(C3):c.2861G>A (p.Arg954His)	C3 (R954H)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 330298	NM_000064.4(C3):c.2857G>A (p.Gly953Ser)	C3 (G953S)	Single nucleotide variant (missense variant)	Age related macular degeneration 9 +2 more	GUncertain significance
Select item 330299	NM_000064.4(C3):c.2799G>A (p.Pro933=)	C3	Single nucleotide variant (synonymous variant)	Age related macular degeneration 9 +3 more	GConflicting classifications of pathogenicity
Select item 892763	NM_000064.4(C3):c.2797-5C>T	C3	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 892765	NM_000064.4(C3):c.2793C>T (p.Val931=)	C3	Single nucleotide variant (synonymous variant)	Complement component 3 deficiency +2 more	GUncertain significance
Select item 330300	NM_000064.4(C3):c.2745T>C (p.Ala915=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 330301	NM_000064.4(C3):c.2715C>T (p.Thr905=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 330302	NM_000064.4(C3):c.2700C>G (p.Ile900Met)	C3 (I900M)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 893862	NM_000064.4(C3):c.2670C>G (p.Pro890=)	C3	Single nucleotide variant (synonymous variant)	C3-related condition +4 more	GConflicting classifications of pathogenicity
Select item 893863	NM_000064.4(C3):c.2646C>T (p.His882=)	C3	Single nucleotide variant (synonymous variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +2 more	GUncertain significance
Select item 894778	NM_000064.4(C3):c.2617T>C (p.Cys873Arg)	C3 (C873R)	Single nucleotide variant (missense variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +2 more	GUncertain significance
Select item 894779	NM_000064.4(C3):c.2584G>T (p.Val862Leu)	C3 (V862L)	Single nucleotide variant (missense variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +2 more	GUncertain significance
Select item 719210	NM_000064.4(C3):c.2583+9C>T	C3	Single nucleotide variant (intron variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 892803	NM_000064.4(C3):c.2441-6G>A	C3	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 330304	NM_000064.4(C3):c.2430G>A (p.Ser810=)	C3	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign
Select item 893609	NM_000064.4(C3):c.2429C>T (p.Ser810Leu)	C3 (S810L)	Single nucleotide variant (missense variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +2 more	GUncertain significance
Select item 330305	NM_000064.4(C3):c.2421G>C (p.Val807=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 330307	NM_000064.4(C3):c.2394C>T (p.Ser798=)	C3	Single nucleotide variant (synonymous variant)	Complement component 3 deficiency +4 more	GBenign/Likely benign
Select item 893893	NM_000064.4(C3):c.2390A>C (p.Asp797Ala)	C3 (D797A)	Single nucleotide variant (missense variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +2 more	GUncertain significance
Select item 330308	NM_000064.4(C3):c.2246-8C>T	C3	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 330309	NM_000064.4(C3):c.2245+15G>A	C3	Single nucleotide variant (intron variant)	Complement component 3 deficiency +3 more	GBenign/Likely benign
Select item 892833	NM_000064.4(C3):c.2207G>A (p.Arg736Gln)	C3 (R736Q)	Single nucleotide variant (missense variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 330310	NM_000064.4(C3):c.2203C>T (p.Arg735Trp)	C3 (R735W)	Single nucleotide variant (missense variant)	Atypical hemolytic-uremic syndrome +5 more	GConflicting classifications of pathogenicity
Select item 330311	NM_000064.4(C3):c.2184C>T (p.Cys728=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 722778	NM_000064.4(C3):c.2157G>A (p.Ala719=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 330312	NM_000064.4(C3):c.2067G>A (p.Glu689=)	C3	Single nucleotide variant (synonymous variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 330314	NM_000064.4(C3):c.1898A>G (p.Lys633Arg)	C3 (K633R)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 330315	NM_000064.4(C3):c.1873A>T (p.Ile625Phe)	C3 (I625F)	Single nucleotide variant (missense variant)	Age related macular degeneration 9 +4 more	GConflicting classifications of pathogenicity
Select item 330316	NM_000064.4(C3):c.1855G>A (p.Val619Met)	C3 (V619M)	Single nucleotide variant (missense variant)	Age related macular degeneration 9 +4 more	GConflicting classifications of pathogenicity
Select item 330317	NM_000064.4(C3):c.1836G>A (p.Thr612=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 330318	NM_000064.4(C3):c.1819A>G (p.Lys607Glu)	C3 (K607E)	Single nucleotide variant (missense variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 330320	NM_000064.4(C3):c.1758G>A (p.Glu586=)	C3	Single nucleotide variant (synonymous variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 892862	NM_000064.4(C3):c.1725T>C (p.Pro575=)	C3	Single nucleotide variant (synonymous variant)	Age related macular degeneration 9 +2 more	GUncertain significance
Select item 330321	NM_000064.4(C3):c.1692G>A (p.Val564=)	C3	Single nucleotide variant (synonymous variant)	Age related macular degeneration 9 +3 more	GBenign
Select item 893674	NM_000064.4(C3):c.1686+10C>T	C3	Single nucleotide variant (intron variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +2 more	GUncertain significance
Select item 893675	NM_000064.4(C3):c.1685C>T (p.Ser562Leu)	C3 (S562L)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 330322	NM_000064.4(C3):c.1653G>T (p.Val551=)	C3	Single nucleotide variant (synonymous variant)	Age related macular degeneration 9 +4 more	GBenign
Select item 330323	NM_000064.4(C3):c.1623C>T (p.Ser541=)	C3	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign/Likely benign
Select item 330324	NM_000064.4(C3):c.1554C>A (p.Pro518=)	C3	Single nucleotide variant (synonymous variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +3 more	GBenign
Select item 893948	NM_000064.4(C3):c.1508C>T (p.Ala503Val)	C3 (A503V)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 894349	NM_000064.4(C3):c.1480-4C>A	C3	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 894350	NM_000064.4(C3):c.1470C>T (p.Tyr490=)	C3	Single nucleotide variant (synonymous variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +3 more	GConflicting classifications of pathogenicity
Select item 330325	NM_000064.4(C3):c.1407G>C (p.Glu469Asp)	C3 (E469D)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 330326	NM_000064.4(C3):c.1303G>A (p.Glu435Lys)	C3 (E435K)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 892903	NM_000064.4(C3):c.1296G>A (p.Ser432=)	C3	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 330327	NM_000064.4(C3):c.1269+14C>A	C3	Single nucleotide variant (intron variant)	Age related macular degeneration 9 +2 more	GUncertain significance
Select item 330328	NM_000064.4(C3):c.1164C>T (p.Pro388=)	C3	Single nucleotide variant (synonymous variant)	Age related macular degeneration 9 +2 more	GConflicting classifications of pathogenicity
Select item 330329	NM_000064.4(C3):c.1119+15G>A	C3	Single nucleotide variant (intron variant)	Complement component 3 deficiency +3 more	GBenign
Select item 330330	NM_000064.4(C3):c.1119+14C>T	C3	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 753058	NM_000064.4(C3):c.1119+10G>A	C3	Single nucleotide variant (intron variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 894380	NM_000064.4(C3):c.1098A>G (p.Pro366=)	C3	Single nucleotide variant (synonymous variant)	Complement component 3 deficiency +3 more	GConflicting classifications of pathogenicity
Select item 330331	NM_000064.4(C3):c.1042A>G (p.Ile348Val)	C3 (I348V)	Single nucleotide variant (missense variant)	Atypical hemolytic-uremic syndrome with C3 anomaly +3 more	GConflicting classifications of pathogenicity

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