rs730880154

Orientation

minus

Stabilized

minus

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

Make rs730880154(A;A)

Make rs730880154(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23433131

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880154
dbSNP (classic)	rs730880154
ClinGen	rs730880154
ebi	rs730880154
HLI	rs730880154
Exac	rs730880154
Gnomad	rs730880154
Varsome	rs730880154
LitVar	rs730880154
Map	rs730880154
PheGenI	rs730880154
Biobank	rs730880154
1000 genomes	rs730880154
hgdp	rs730880154
ensembl	rs730880154
geneview	rs730880154
scholar	rs730880154
google	rs730880154
pharmgkb	rs730880154
gwascentral	rs730880154
openSNP	rs730880154
23andMe	rs730880154
SNPshot	rs730880154
SNPdbe	rs730880154
MSV3d	rs730880154
GWAS Ctlg	rs730880154

Max Magnitude

0

ClinVar
Risk	rs730880154(A;A) rs730880154(T;T)
Alt	rs730880154(A;A) rs730880154(T;T)
Reference	Rs730880154(G;G)
Significance	Probable-Pathogenic
Disease	Cardiomyopathy not specified
Variation	info
Gene	MYH7
CLNDBN	Cardiomyopathy, restrictive not specified
Reversed	1
HGVS	NC_000014.8:g.23902340C>T
CLNSRC
CLNACC	RCV000157347.1, RCV000455842.1,