rs730880921

Orientation

minus

Stabilized

minus

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

Make rs730880921(C;G)

Make rs730880921(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23431592

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880921
dbSNP (classic)	rs730880921
ClinGen	rs730880921
ebi	rs730880921
HLI	rs730880921
Exac	rs730880921
Gnomad	rs730880921
Varsome	rs730880921
LitVar	rs730880921
Map	rs730880921
PheGenI	rs730880921
Biobank	rs730880921
1000 genomes	rs730880921
hgdp	rs730880921
ensembl	rs730880921
geneview	rs730880921
scholar	rs730880921
google	rs730880921
pharmgkb	rs730880921
gwascentral	rs730880921
openSNP	rs730880921
23andMe	rs730880921
SNPshot	rs730880921
SNPdbe	rs730880921
MSV3d	rs730880921
GWAS Ctlg	rs730880921

Max Magnitude

0

ClinVar
Risk	rs730880921(G;G)
Alt	rs730880921(G;G)
Reference	Rs730880921(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23900801G>C
CLNSRC
CLNACC	RCV000158880.1,