rs398123913

Orientation

minus

Stabilized

minus

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

Make rs398123913(-;-)

Make rs398123913(-;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

33211285

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123913
dbSNP (classic)	rs398123913
ClinGen	rs398123913
ebi	rs398123913
HLI	rs398123913
Exac	rs398123913
Gnomad	rs398123913
Varsome	rs398123913
LitVar	rs398123913
Map	rs398123913
PheGenI	rs398123913
Biobank	rs398123913
1000 genomes	rs398123913
hgdp	rs398123913
ensembl	rs398123913
geneview	rs398123913
scholar	rs398123913
google	rs398123913
pharmgkb	rs398123913
gwascentral	rs398123913
openSNP	rs398123913
23andMe	rs398123913
SNPshot	rs398123913
SNPdbe	rs398123913
MSV3d	rs398123913
GWAS Ctlg	rs398123913

Max Magnitude

0

ClinVar
Risk	rs398123913(-;-)
Alt	rs398123913(-;-)
Reference	Rs398123913(T;T)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.33229402delA
CLNSRC	ClinVar
CLNACC	RCV000080531.4, RCV000173320.1, RCV000173321.1,