rs121913634

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	6.2	Familial Hypertrophic Cardiomyopathy
(A;T)	6.2	Familial Hypertrophic Cardiomyopathy

Make rs121913634(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23425372

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs121913634
dbSNP (classic)	rs121913634
ClinGen	rs121913634
ebi	rs121913634
HLI	rs121913634
Exac	rs121913634
Gnomad	rs121913634
Varsome	rs121913634
LitVar	rs121913634
Map	rs121913634
PheGenI	rs121913634
Biobank	rs121913634
1000 genomes	rs121913634
hgdp	rs121913634
ensembl	rs121913634
geneview	rs121913634
scholar	rs121913634
google	rs121913634
pharmgkb	rs121913634
gwascentral	rs121913634
openSNP	rs121913634
23andMe	rs121913634
SNPshot	rs121913634
SNPdbe	rs121913634
MSV3d	rs121913634
GWAS Ctlg	rs121913634

Max Magnitude

6.2

OMIM	160760
Desc
Variant	0013
Related	also

ClinVar
Risk	rs121913634(G;G)
Alt	rs121913634(G;G)
Reference	Rs121913634(A;A)
Significance	Pathogenic
Disease	Familial hypertrophic cardiomyopathy 1 not specified
Variation	info
Gene	MYH7
CLNDBN	Familial hypertrophic cardiomyopathy 1 not specified
Reversed	1
HGVS	NC_000014.8:g.23894581T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015156.26, RCV000168868.2,