rs606231315

Orientation

plus

Stabilized

plus

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

Make rs606231315(C;T)

Make rs606231315(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23431678

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs606231315
dbSNP (classic)	rs606231315
ClinGen	rs606231315
ebi	rs606231315
HLI	rs606231315
Exac	rs606231315
Gnomad	rs606231315
Varsome	rs606231315
LitVar	rs606231315
Map	rs606231315
PheGenI	rs606231315
Biobank	rs606231315
1000 genomes	rs606231315
hgdp	rs606231315
ensembl	rs606231315
geneview	rs606231315
scholar	rs606231315
google	rs606231315
pharmgkb	rs606231315
gwascentral	rs606231315
openSNP	rs606231315
23andMe	rs606231315
SNPshot	rs606231315
SNPdbe	rs606231315
MSV3d	rs606231315
GWAS Ctlg	rs606231315

Max Magnitude

0

ClinVar
Risk	rs606231315(T;T)
Alt	rs606231315(T;T)
Reference	Rs606231315(C;C)
Significance	Probable-Pathogenic
Disease	Familial cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Familial cardiomyopathy
Reversed	0
HGVS	NC_000014.8:g.23900887C>T
CLNSRC
CLNACC	RCV000148983.1,