rs606231340

Orientation

plus

Stabilized

plus

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

Make rs606231340(C;T)

Make rs606231340(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424143

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs606231340
dbSNP (classic)	rs606231340
ClinGen	rs606231340
ebi	rs606231340
HLI	rs606231340
Exac	rs606231340
Gnomad	rs606231340
Varsome	rs606231340
LitVar	rs606231340
Map	rs606231340
PheGenI	rs606231340
Biobank	rs606231340
1000 genomes	rs606231340
hgdp	rs606231340
ensembl	rs606231340
geneview	rs606231340
scholar	rs606231340
google	rs606231340
pharmgkb	rs606231340
gwascentral	rs606231340
openSNP	rs606231340
23andMe	rs606231340
SNPshot	rs606231340
SNPdbe	rs606231340
MSV3d	rs606231340
GWAS Ctlg	rs606231340

Max Magnitude

0

ClinVar
Risk	rs606231340(T;T)
Alt	rs606231340(T;T)
Reference	Rs606231340(C;C)
Significance	Pathogenic
Disease	Familial cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Familial cardiomyopathy
Reversed	0
HGVS	NC_000014.8:g.23893352C>T
CLNSRC
CLNACC	RCV000148955.1,