rs730880729

Orientation

minus

Stabilized

minus

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

Make rs730880729(A;A)

Make rs730880729(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23432768

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880729
dbSNP (classic)	rs730880729
ClinGen	rs730880729
ebi	rs730880729
HLI	rs730880729
Exac	rs730880729
Gnomad	rs730880729
Varsome	rs730880729
LitVar	rs730880729
Map	rs730880729
PheGenI	rs730880729
Biobank	rs730880729
1000 genomes	rs730880729
hgdp	rs730880729
ensembl	rs730880729
geneview	rs730880729
scholar	rs730880729
google	rs730880729
pharmgkb	rs730880729
gwascentral	rs730880729
openSNP	rs730880729
23andMe	rs730880729
SNPshot	rs730880729
SNPdbe	rs730880729
MSV3d	rs730880729
GWAS Ctlg	rs730880729

Max Magnitude

0

ClinVar
Risk	rs730880729(A;A) rs730880729(T;T)
Alt	rs730880729(A;A) rs730880729(T;T)
Reference	Rs730880729(G;G)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23901977C>A; NC_000014.8:g.23901977C>T
CLNSRC
CLNACC	RCV000158729.2, RCV000158501.1,