rs730880877

Orientation

minus

Stabilized

minus

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

Make rs730880877(A;G)

Make rs730880877(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23427866

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880877
dbSNP (classic)	rs730880877
ClinGen	rs730880877
ebi	rs730880877
HLI	rs730880877
Exac	rs730880877
Gnomad	rs730880877
Varsome	rs730880877
LitVar	rs730880877
Map	rs730880877
PheGenI	rs730880877
Biobank	rs730880877
1000 genomes	rs730880877
hgdp	rs730880877
ensembl	rs730880877
geneview	rs730880877
scholar	rs730880877
google	rs730880877
pharmgkb	rs730880877
gwascentral	rs730880877
openSNP	rs730880877
23andMe	rs730880877
SNPshot	rs730880877
SNPdbe	rs730880877
MSV3d	rs730880877
GWAS Ctlg	rs730880877

Max Magnitude

0

ClinVar
Risk	rs730880877(G;G)
Alt	rs730880877(G;G)
Reference	Rs730880877(A;A)
Significance	Probable-Pathogenic
Disease	Cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23897075T>C
CLNSRC
CLNACC	RCV000158811.1,