rs730880900

Orientation

minus

Stabilized

minus

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

Make rs730880900(C;C)

Make rs730880900(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424106

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880900
dbSNP (classic)	rs730880900
ClinGen	rs730880900
ebi	rs730880900
HLI	rs730880900
Exac	rs730880900
Gnomad	rs730880900
Varsome	rs730880900
LitVar	rs730880900
Map	rs730880900
PheGenI	rs730880900
Biobank	rs730880900
1000 genomes	rs730880900
hgdp	rs730880900
ensembl	rs730880900
geneview	rs730880900
scholar	rs730880900
google	rs730880900
pharmgkb	rs730880900
gwascentral	rs730880900
openSNP	rs730880900
23andMe	rs730880900
SNPshot	rs730880900
SNPdbe	rs730880900
MSV3d	rs730880900
GWAS Ctlg	rs730880900

Max Magnitude

0

ClinVar
Risk	rs730880900(C;C)
Alt	rs730880900(C;C)
Reference	Rs730880900(T;T)
Significance	Pathogenic
Disease	Cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	Cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23893315A>G
CLNSRC
CLNACC	RCV000158849.1,