rs1057524857

Orientation

minus

Stabilized

minus

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

Make rs1057524857(A;A)

Make rs1057524857(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

23425977

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs1057524857
dbSNP (classic)	rs1057524857
ClinGen	rs1057524857
ebi	rs1057524857
HLI	rs1057524857
Exac	rs1057524857
Gnomad	rs1057524857
Varsome	rs1057524857
LitVar	rs1057524857
Map	rs1057524857
PheGenI	rs1057524857
Biobank	rs1057524857
1000 genomes	rs1057524857
hgdp	rs1057524857
ensembl	rs1057524857
geneview	rs1057524857
scholar	rs1057524857
google	rs1057524857
pharmgkb	rs1057524857
gwascentral	rs1057524857
openSNP	rs1057524857
23andMe	rs1057524857
SNPshot	rs1057524857
SNPdbe	rs1057524857
MSV3d	rs1057524857
GWAS Ctlg	rs1057524857

Max Magnitude

0

ClinVar
Risk	rs1057524857(A;A)
Alt	rs1057524857(A;A)
Reference	Rs1057524857(G;G)
Significance	Probable-Pathogenic
Disease	not provided Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	not provided Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23895186C>T
CLNSRC
CLNACC	RCV000429496.1, RCV000460699.1,