rs587782961

Orientation

minus

Stabilized

minus

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

Make rs587782961(A;G)

Make rs587782961(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23430936

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs587782961
dbSNP (classic)	rs587782961
ClinGen	rs587782961
ebi	rs587782961
HLI	rs587782961
Exac	rs587782961
Gnomad	rs587782961
Varsome	rs587782961
LitVar	rs587782961
Map	rs587782961
PheGenI	rs587782961
Biobank	rs587782961
1000 genomes	rs587782961
hgdp	rs587782961
ensembl	rs587782961
geneview	rs587782961
scholar	rs587782961
google	rs587782961
pharmgkb	rs587782961
gwascentral	rs587782961
openSNP	rs587782961
23andMe	rs587782961
SNPshot	rs587782961
SNPdbe	rs587782961
MSV3d	rs587782961
GWAS Ctlg	rs587782961

Max Magnitude

0

ClinVar
Risk	rs587782961(G;G)
Alt	rs587782961(G;G)
Reference	Rs587782961(A;A)
Significance	Probable-Pathogenic
Disease	Left ventricular noncompaction cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Left ventricular noncompaction cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23900145T>C
CLNSRC
CLNACC	RCV000143920.1,