rs606231329

Orientation

plus

Stabilized

plus

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

Make rs606231329(A;C)

Make rs606231329(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23427238

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs606231329
dbSNP (classic)	rs606231329
ClinGen	rs606231329
ebi	rs606231329
HLI	rs606231329
Exac	rs606231329
Gnomad	rs606231329
Varsome	rs606231329
LitVar	rs606231329
Map	rs606231329
PheGenI	rs606231329
Biobank	rs606231329
1000 genomes	rs606231329
hgdp	rs606231329
ensembl	rs606231329
geneview	rs606231329
scholar	rs606231329
google	rs606231329
pharmgkb	rs606231329
gwascentral	rs606231329
openSNP	rs606231329
23andMe	rs606231329
SNPshot	rs606231329
SNPdbe	rs606231329
MSV3d	rs606231329
GWAS Ctlg	rs606231329

Max Magnitude

0

ClinVar
Risk	rs606231329(C;C)
Alt	rs606231329(C;C)
Reference	Rs606231329(A;A)
Significance	Pathogenic
Disease	Familial cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Familial cardiomyopathy
Reversed	0
HGVS	NC_000014.8:g.23896447A>C
CLNSRC
CLNACC	RCV000148969.1,