rs730880880

Orientation

minus

Stabilized

minus

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

Make rs730880880(A;G)

Make rs730880880(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23427668

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880880
dbSNP (classic)	rs730880880
ClinGen	rs730880880
ebi	rs730880880
HLI	rs730880880
Exac	rs730880880
Gnomad	rs730880880
Varsome	rs730880880
LitVar	rs730880880
Map	rs730880880
PheGenI	rs730880880
Biobank	rs730880880
1000 genomes	rs730880880
hgdp	rs730880880
ensembl	rs730880880
geneview	rs730880880
scholar	rs730880880
google	rs730880880
pharmgkb	rs730880880
gwascentral	rs730880880
openSNP	rs730880880
23andMe	rs730880880
SNPshot	rs730880880
SNPdbe	rs730880880
MSV3d	rs730880880
GWAS Ctlg	rs730880880

Max Magnitude

0

ClinVar
Risk	rs730880880(G;G)
Alt	rs730880880(G;G)
Reference	Rs730880880(A;A)
Significance	Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23896877T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000158817.2,