rs606231319

Orientation

plus

Stabilized

plus

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

Make rs606231319(G;T)

Make rs606231319(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23429335

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs606231319
dbSNP (classic)	rs606231319
ClinGen	rs606231319
ebi	rs606231319
HLI	rs606231319
Exac	rs606231319
Gnomad	rs606231319
Varsome	rs606231319
LitVar	rs606231319
Map	rs606231319
PheGenI	rs606231319
Biobank	rs606231319
1000 genomes	rs606231319
hgdp	rs606231319
ensembl	rs606231319
geneview	rs606231319
scholar	rs606231319
google	rs606231319
pharmgkb	rs606231319
gwascentral	rs606231319
openSNP	rs606231319
23andMe	rs606231319
SNPshot	rs606231319
SNPdbe	rs606231319
MSV3d	rs606231319
GWAS Ctlg	rs606231319

Max Magnitude

0

ClinVar
Risk	rs606231319(T;T)
Alt	rs606231319(T;T)
Reference	Rs606231319(G;G)
Significance	Pathogenic
Disease	Familial cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Familial cardiomyopathy
Reversed	0
HGVS	NC_000014.8:g.23898544G>T
CLNSRC
CLNACC	RCV000148979.1,