rs398123865

Orientation

minus

Stabilized

minus

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

Make rs398123865(C;T)

Make rs398123865(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32573834

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123865
dbSNP (classic)	rs398123865
ClinGen	rs398123865
ebi	rs398123865
HLI	rs398123865
Exac	rs398123865
Gnomad	rs398123865
Varsome	rs398123865
LitVar	rs398123865
Map	rs398123865
PheGenI	rs398123865
Biobank	rs398123865
1000 genomes	rs398123865
hgdp	rs398123865
ensembl	rs398123865
geneview	rs398123865
scholar	rs398123865
google	rs398123865
pharmgkb	rs398123865
gwascentral	rs398123865
openSNP	rs398123865
23andMe	rs398123865
SNPshot	rs398123865
SNPdbe	rs398123865
MSV3d	rs398123865
GWAS Ctlg	rs398123865

Max Magnitude

0

ClinVar
Risk	rs398123865(T;T)
Alt	rs398123865(T;T)
Reference	Rs398123865(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.32591951G>A
CLNSRC	HGMD
CLNACC	RCV000080461.4, RCV000174744.1, RCV000174745.2,