rs730880881

Orientation

minus

Stabilized

minus

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

Make rs730880881(C;T)

Make rs730880881(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23427662

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880881
dbSNP (classic)	rs730880881
ClinGen	rs730880881
ebi	rs730880881
HLI	rs730880881
Exac	rs730880881
Gnomad	rs730880881
Varsome	rs730880881
LitVar	rs730880881
Map	rs730880881
PheGenI	rs730880881
Biobank	rs730880881
1000 genomes	rs730880881
hgdp	rs730880881
ensembl	rs730880881
geneview	rs730880881
scholar	rs730880881
google	rs730880881
pharmgkb	rs730880881
gwascentral	rs730880881
openSNP	rs730880881
23andMe	rs730880881
SNPshot	rs730880881
SNPdbe	rs730880881
MSV3d	rs730880881
GWAS Ctlg	rs730880881

Max Magnitude

0

ClinVar
Risk	rs730880881(T;T)
Alt	rs730880881(T;T)
Reference	Rs730880881(C;C)
Significance	Probable-Pathogenic
Disease	Cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23896871G>A
CLNSRC
CLNACC	RCV000158818.1,