rs398123895

Orientation

minus

Stabilized

minus

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

Make rs398123895(-;-)

Make rs398123895(-;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32491352

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123895
dbSNP (classic)	rs398123895
ClinGen	rs398123895
ebi	rs398123895
HLI	rs398123895
Exac	rs398123895
Gnomad	rs398123895
Varsome	rs398123895
LitVar	rs398123895
Map	rs398123895
PheGenI	rs398123895
Biobank	rs398123895
1000 genomes	rs398123895
hgdp	rs398123895
ensembl	rs398123895
geneview	rs398123895
scholar	rs398123895
google	rs398123895
pharmgkb	rs398123895
gwascentral	rs398123895
openSNP	rs398123895
23andMe	rs398123895
SNPshot	rs398123895
SNPdbe	rs398123895
MSV3d	rs398123895
GWAS Ctlg	rs398123895

Max Magnitude

0

ClinVar
Risk	rs398123895(-;-)
Alt	rs398123895(-;-)
Reference	Rs398123895(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.32509469delA
CLNSRC	ClinVar
CLNACC	RCV000080508.4, RCV000176075.1, RCV000176076.1,