rs186964570

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs186964570(A;A)

Make rs186964570(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23433656

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs186964570
dbSNP (classic)	rs186964570
ClinGen	rs186964570
ebi	rs186964570
HLI	rs186964570
Exac	rs186964570
Gnomad	rs186964570
Varsome	rs186964570
LitVar	rs186964570
Map	rs186964570
PheGenI	rs186964570
Biobank	rs186964570
1000 genomes	rs186964570
hgdp	rs186964570
ensembl	rs186964570
geneview	rs186964570
scholar	rs186964570
google	rs186964570
pharmgkb	rs186964570
gwascentral	rs186964570
openSNP	rs186964570
23andMe	rs186964570
SNPshot	rs186964570
SNPdbe	rs186964570
MSV3d	rs186964570
GWAS Ctlg	rs186964570

Max Magnitude

0

ClinVar
Risk	rs186964570(A;A)
Alt	rs186964570(A;A)
Reference	Rs186964570(G;G)
Significance	Other
Disease	not specified Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 1 Myosin storage myopathy Hypertrophic cardiomyopathy Dilated Cardiomyopathy Left ventricular noncompaction cardiomyopathy Laing distal myopathy Scapuloperoneal myopathy
Variation	info
Gene	MYH7
CLNDBN	not specified Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 1 Myosin storage myopathy Hypertrophic cardiomyopathy Dilated Cardiomyopathy, Dominant Left ventricular noncompaction cardiomyopathy Laing distal myopathy Scapuloperoneal myopathy
Reversed	0
HGVS	NC_000014.8:g.23902865G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000036003.3, RCV000148713.3, RCV000168831.3, RCV000264317.1, RCV000279740.1, RCV000319538.1, RCV000334846.1, RCV000374158.1, RCV000377499.1,