rs398124057

Orientation

minus

Stabilized

minus

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

Make rs398124057(-;-)

Make rs398124057(-;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31679393

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124057
dbSNP (classic)	rs398124057
ClinGen	rs398124057
ebi	rs398124057
HLI	rs398124057
Exac	rs398124057
Gnomad	rs398124057
Varsome	rs398124057
LitVar	rs398124057
Map	rs398124057
PheGenI	rs398124057
Biobank	rs398124057
1000 genomes	rs398124057
hgdp	rs398124057
ensembl	rs398124057
geneview	rs398124057
scholar	rs398124057
google	rs398124057
pharmgkb	rs398124057
gwascentral	rs398124057
openSNP	rs398124057
23andMe	rs398124057
SNPshot	rs398124057
SNPdbe	rs398124057
MSV3d	rs398124057
GWAS Ctlg	rs398124057

Max Magnitude

0

ClinVar
Risk	rs398124057(-;-)
Alt	rs398124057(-;-)
Reference	Rs398124057(G;G)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.31697510delC
CLNSRC	ClinVar
CLNACC	RCV000080773.3,