rs398123903

Orientation

minus

Stabilized

minus

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

Make rs398123903(C;T)

Make rs398123903(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32485072

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123903
dbSNP (classic)	rs398123903
ClinGen	rs398123903
ebi	rs398123903
HLI	rs398123903
Exac	rs398123903
Gnomad	rs398123903
Varsome	rs398123903
LitVar	rs398123903
Map	rs398123903
PheGenI	rs398123903
Biobank	rs398123903
1000 genomes	rs398123903
hgdp	rs398123903
ensembl	rs398123903
geneview	rs398123903
scholar	rs398123903
google	rs398123903
pharmgkb	rs398123903
gwascentral	rs398123903
openSNP	rs398123903
23andMe	rs398123903
SNPshot	rs398123903
SNPdbe	rs398123903
MSV3d	rs398123903
GWAS Ctlg	rs398123903

Max Magnitude

0

ClinVar
Risk	rs398123903(T;T)
Alt	rs398123903(T;T)
Reference	Rs398123903(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.32503189G>A
CLNSRC	HGMD
CLNACC	RCV000080518.4, RCV000176202.1, RCV000176203.1,