rs515726230

Orientation

minus

Stabilized

minus

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

Make rs515726230(A;G)

Make rs515726230(G;G)

Reference

GRCh38 38.1/142

Chromosome

14

Position

23397187

Gene

MYH6

is a	snp
is	mentioned by
dbSNP	rs515726230
dbSNP (classic)	rs515726230
ClinGen	rs515726230
ebi	rs515726230
HLI	rs515726230
Exac	rs515726230
Gnomad	rs515726230
Varsome	rs515726230
LitVar	rs515726230
Map	rs515726230
PheGenI	rs515726230
Biobank	rs515726230
1000 genomes	rs515726230
hgdp	rs515726230
ensembl	rs515726230
geneview	rs515726230
scholar	rs515726230
google	rs515726230
pharmgkb	rs515726230
gwascentral	rs515726230
openSNP	rs515726230
23andMe	rs515726230
SNPshot	rs515726230
SNPdbe	rs515726230
MSV3d	rs515726230
GWAS Ctlg	rs515726230

Max Magnitude

0

ClinVar
Risk	rs515726230(G;G)
Alt	rs515726230(G;G)
Reference	Rs515726230(A;A)
Significance	Probable-Pathogenic
Disease	Heart
Variation	info
Gene	MYH6
CLNDBN	Heart, malformation of
Reversed	1
HGVS	NC_000014.8:g.23866396T>C
CLNSRC	ClinVar
CLNACC	RCV000128628.1,