rs398123867

Orientation

minus

Stabilized

minus

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

Make rs398123867(A;A)

Make rs398123867(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32565808

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123867
dbSNP (classic)	rs398123867
ClinGen	rs398123867
ebi	rs398123867
HLI	rs398123867
Exac	rs398123867
Gnomad	rs398123867
Varsome	rs398123867
LitVar	rs398123867
Map	rs398123867
PheGenI	rs398123867
Biobank	rs398123867
1000 genomes	rs398123867
hgdp	rs398123867
ensembl	rs398123867
geneview	rs398123867
scholar	rs398123867
google	rs398123867
pharmgkb	rs398123867
gwascentral	rs398123867
openSNP	rs398123867
23andMe	rs398123867
SNPshot	rs398123867
SNPdbe	rs398123867
MSV3d	rs398123867
GWAS Ctlg	rs398123867

Max Magnitude

0

ClinVar
Risk	rs398123867(A;A)
Alt	rs398123867(A;A)
Reference	Rs398123867(C;C)
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.32583925G>T
CLNSRC	ClinVar Emory University
CLNACC	RCV000080469.4, RCV000175052.1, RCV000175053.1,