rs398124059

Orientation

minus

Stabilized

minus

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

Make rs398124059(-;-)

Make rs398124059(-;A)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31658095

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124059
dbSNP (classic)	rs398124059
ClinGen	rs398124059
ebi	rs398124059
HLI	rs398124059
Exac	rs398124059
Gnomad	rs398124059
Varsome	rs398124059
LitVar	rs398124059
Map	rs398124059
PheGenI	rs398124059
Biobank	rs398124059
1000 genomes	rs398124059
hgdp	rs398124059
ensembl	rs398124059
geneview	rs398124059
scholar	rs398124059
google	rs398124059
pharmgkb	rs398124059
gwascentral	rs398124059
openSNP	rs398124059
23andMe	rs398124059
SNPshot	rs398124059
SNPdbe	rs398124059
MSV3d	rs398124059
GWAS Ctlg	rs398124059

Max Magnitude

0

ClinVar
Risk	rs398124059(-;-)
Alt	rs398124059(-;-)
Reference	Rs398124059(A;A)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.31676212delT
CLNSRC	ClinVar
CLNACC	RCV000080775.3,