rs398123870

Orientation

minus

Stabilized

minus

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

Make rs398123870(C;T)

Make rs398123870(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32565704

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123870
dbSNP (classic)	rs398123870
ClinGen	rs398123870
ebi	rs398123870
HLI	rs398123870
Exac	rs398123870
Gnomad	rs398123870
Varsome	rs398123870
LitVar	rs398123870
Map	rs398123870
PheGenI	rs398123870
Biobank	rs398123870
1000 genomes	rs398123870
hgdp	rs398123870
ensembl	rs398123870
geneview	rs398123870
scholar	rs398123870
google	rs398123870
pharmgkb	rs398123870
gwascentral	rs398123870
openSNP	rs398123870
23andMe	rs398123870
SNPshot	rs398123870
SNPdbe	rs398123870
MSV3d	rs398123870
GWAS Ctlg	rs398123870

Max Magnitude

0

ClinVar
Risk	rs398123870(T;T)
Alt	rs398123870(T;T)
Reference	Rs398123870(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.32583821G>A
CLNSRC	HGMD
CLNACC	RCV000080473.4, RCV000175054.1, RCV000175055.1,