rs398123872

Orientation

minus

Stabilized

minus

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

Make rs398123872(C;T)

Make rs398123872(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32545295

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123872
dbSNP (classic)	rs398123872
ClinGen	rs398123872
ebi	rs398123872
HLI	rs398123872
Exac	rs398123872
Gnomad	rs398123872
Varsome	rs398123872
LitVar	rs398123872
Map	rs398123872
PheGenI	rs398123872
Biobank	rs398123872
1000 genomes	rs398123872
hgdp	rs398123872
ensembl	rs398123872
geneview	rs398123872
scholar	rs398123872
google	rs398123872
pharmgkb	rs398123872
gwascentral	rs398123872
openSNP	rs398123872
23andMe	rs398123872
SNPshot	rs398123872
SNPdbe	rs398123872
MSV3d	rs398123872
GWAS Ctlg	rs398123872

Max Magnitude

0

ClinVar
Risk	rs398123872(G;G) rs398123872(T;T)
Alt	rs398123872(G;G) rs398123872(T;T)
Reference	Rs398123872(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.32563412G>A
CLNSRC	ClinVar Emory University
CLNACC	RCV000080476.4, RCV000175181.1, RCV000175182.1,