rs730880917

Orientation

minus

Stabilized

minus

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

Make rs730880917(C;C)

Make rs730880917(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23415156

Gene	MHRT, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880917
dbSNP (classic)	rs730880917
ClinGen	rs730880917
ebi	rs730880917
HLI	rs730880917
Exac	rs730880917
Gnomad	rs730880917
Varsome	rs730880917
LitVar	rs730880917
Map	rs730880917
PheGenI	rs730880917
Biobank	rs730880917
1000 genomes	rs730880917
hgdp	rs730880917
ensembl	rs730880917
geneview	rs730880917
scholar	rs730880917
google	rs730880917
pharmgkb	rs730880917
gwascentral	rs730880917
openSNP	rs730880917
23andMe	rs730880917
SNPshot	rs730880917
SNPdbe	rs730880917
MSV3d	rs730880917
GWAS Ctlg	rs730880917

Max Magnitude

0

ClinVar
Risk	rs730880917(C;C)
Alt	rs730880917(C;C)
Reference	Rs730880917(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7 MHRT
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23884365C>G
CLNSRC
CLNACC	RCV000158873.1,