ClinVar (all) for Orgtrack (Select 507090) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 638684	NM_020884.7(MYH7B):c.4931_4932del (p.Thr1644fs)	MYH7B (T1644fs)	Microsatellite (frameshift variant)	Hypertrophic cardiomyopathy 1	GPathogenic
Select item 638683	NM_020884.7(MYH7B):c.624+1G>A	MYH7B	Single nucleotide variant (splice donor variant)	Hypertrophic cardiomyopathy 1	GPathogenic
Select item 638682	NM_020884.7(MYH7B):c.611_615dup (p.Lys206fs)	MYH7B (K206fs)	Microsatellite (frameshift variant)	Hypertrophic cardiomyopathy 1	GPathogenic
Select item 638681	NM_020884.7(MYH7B):c.5335G>C (p.Glu1779Gln)	MYH7B (E1779Q)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 1	GLikely pathogenic
Select item 638680	NM_020884.7(MYH7B):c.4415G>A (p.Arg1472Gln)	MYH7B (R1472Q)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 1	GLikely pathogenic
Select item 638679	NM_020884.7(MYH7B):c.2719G>C (p.Asp907His)	MYH7B (D907H)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 1	GLikely pathogenic
Select item 638678	NM_020884.7(MYH7B):c.1837T>C (p.Phe613Leu)	MYH7B (F613L)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 1	GLikely pathogenic

ClinVar