"Illumina Laboratory Services, Illumina"[submitter] AND "LOC126861898" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 177847	NM_000257.4(MYH7):c.2602G>C (p.Ala868Pro)	LOC126861898, MYH7 (A868P)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy	GLikely pathogenic FDA Recognized database
Select item 181161	NM_000257.4(MYH7):c.2526T>C (p.Ser842=)	LOC126861898, MYH7	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy +8 more	GConflicting classifications of pathogenicity
Select item 882969	NM_000257.4(MYH7):c.2424-7C>T	LOC126861898, MYH7	Single nucleotide variant (intron variant)	Myosin storage myopathy +5 more	GConflicting classifications of pathogenicity
Select item 42900	NM_000257.4(MYH7):c.2360G>A (p.Arg787His)	LOC126861898, MYH7 (R787H)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy	GLikely benign FDA Recognized database
Select item 161327	NM_000257.4(MYH7):c.2359C>T (p.Arg787Cys)	LOC126861898, MYH7 (R787C)	Single nucleotide variant (missense variant)	not specified +7 more	GConflicting classifications of pathogenicity
Select item 42896	NM_000257.4(MYH7):c.2349C>T (p.Arg783=)	LOC126861898, MYH7	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 1 +9 more	GBenign/Likely benign
Select item 42894	NM_000257.4(MYH7):c.2334C>T (p.Asp778=)	LOC126861898, MYH7	Single nucleotide variant (synonymous variant)	Myosin storage myopathy +8 more	GConflicting classifications of pathogenicity

ClinVar