rs730880846

Orientation

minus

Stabilized

minus

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

Make rs730880846(A;G)

Make rs730880846(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23431783

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880846
dbSNP (classic)	rs730880846
ClinGen	rs730880846
ebi	rs730880846
HLI	rs730880846
Exac	rs730880846
Gnomad	rs730880846
Varsome	rs730880846
LitVar	rs730880846
Map	rs730880846
PheGenI	rs730880846
Biobank	rs730880846
1000 genomes	rs730880846
hgdp	rs730880846
ensembl	rs730880846
geneview	rs730880846
scholar	rs730880846
google	rs730880846
pharmgkb	rs730880846
gwascentral	rs730880846
openSNP	rs730880846
23andMe	rs730880846
SNPshot	rs730880846
SNPdbe	rs730880846
MSV3d	rs730880846
GWAS Ctlg	rs730880846

Max Magnitude

0

ClinVar
Risk	rs730880846(G;G)
Alt	rs730880846(G;G)
Reference	Rs730880846(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23900992T>C
CLNSRC
CLNACC	RCV000158751.2,