rs730880925

Orientation

minus

Stabilized

minus

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

Make rs730880925(C;C)

Make rs730880925(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23429309

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880925
dbSNP (classic)	rs730880925
ClinGen	rs730880925
ebi	rs730880925
HLI	rs730880925
Exac	rs730880925
Gnomad	rs730880925
Varsome	rs730880925
LitVar	rs730880925
Map	rs730880925
PheGenI	rs730880925
Biobank	rs730880925
1000 genomes	rs730880925
hgdp	rs730880925
ensembl	rs730880925
geneview	rs730880925
scholar	rs730880925
google	rs730880925
pharmgkb	rs730880925
gwascentral	rs730880925
openSNP	rs730880925
23andMe	rs730880925
SNPshot	rs730880925
SNPdbe	rs730880925
MSV3d	rs730880925
GWAS Ctlg	rs730880925

Max Magnitude

0

ClinVar
Risk	rs730880925(C;C)
Alt	rs730880925(C;C)
Reference	Rs730880925(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23898518C>G
CLNSRC
CLNACC	RCV000158884.4,