rs730880915

Orientation

minus

Stabilized

minus

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

Make rs730880915(C;T)

Make rs730880915(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23415721

Gene	MHRT, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880915
dbSNP (classic)	rs730880915
ClinGen	rs730880915
ebi	rs730880915
HLI	rs730880915
Exac	rs730880915
Gnomad	rs730880915
Varsome	rs730880915
LitVar	rs730880915
Map	rs730880915
PheGenI	rs730880915
Biobank	rs730880915
1000 genomes	rs730880915
hgdp	rs730880915
ensembl	rs730880915
geneview	rs730880915
scholar	rs730880915
google	rs730880915
pharmgkb	rs730880915
gwascentral	rs730880915
openSNP	rs730880915
23andMe	rs730880915
SNPshot	rs730880915
SNPdbe	rs730880915
MSV3d	rs730880915
GWAS Ctlg	rs730880915

Max Magnitude

0

ClinVar
Risk	rs730880915(G;G) rs730880915(T;T)
Alt	rs730880915(G;G) rs730880915(T;T)
Reference	Rs730880915(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7 MHRT
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23884930G>A
CLNSRC
CLNACC	RCV000158870.3,