C1858380[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1649036	NM_001040108.2(MLH3):c.4011+15T>G	MLH3	Single nucleotide variant (intron variant)	Endometrial carcinoma +3 more	GBenign/Likely benign
Select item 1372959	NM_001040108.2(MLH3):c.3676G>A (p.Ala1226Thr)	MLH3 (A1226T)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GUncertain significance
Select item 238248	NM_001040108.2(MLH3):c.3137G>A (p.Arg1046Gln)	MLH3 (R1046Q)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 410896	NM_001040108.2(MLH3):c.2911G>A (p.Val971Ile)	MLH3 (V971I)	Single nucleotide variant (missense variant)	MLH3-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 1384629	NM_001040108.2(MLH3):c.2000G>C (p.Gly667Ala)	MLH3 (G667A)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 701298	NM_001040108.2(MLH3):c.873T>G (p.Asn291Lys)	MLH3 (N291K)	Single nucleotide variant (missense variant)	Colorectal cancer, hereditary nonpolyposis, type 7 +3 more	GConflicting classifications of pathogenicity
Select item 660075	NM_001040108.2(MLH3):c.443T>C (p.Val148Ala)	MLH3 (V148A)	Single nucleotide variant (missense variant)	Endometrial carcinoma +3 more	GUncertain significance

ClinVar