rs398123981

Orientation

minus

Stabilized

minus

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

Make rs398123981(C;T)

Make rs398123981(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32362826

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123981
dbSNP (classic)	rs398123981
ClinGen	rs398123981
ebi	rs398123981
HLI	rs398123981
Exac	rs398123981
Gnomad	rs398123981
Varsome	rs398123981
LitVar	rs398123981
Map	rs398123981
PheGenI	rs398123981
Biobank	rs398123981
1000 genomes	rs398123981
hgdp	rs398123981
ensembl	rs398123981
geneview	rs398123981
scholar	rs398123981
google	rs398123981
pharmgkb	rs398123981
gwascentral	rs398123981
openSNP	rs398123981
23andMe	rs398123981
SNPshot	rs398123981
SNPdbe	rs398123981
MSV3d	rs398123981
GWAS Ctlg	rs398123981

Max Magnitude

0

ClinVar
Risk	rs398123981(T;T)
Alt	rs398123981(T;T)
Reference	Rs398123981(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.32380943G>A
CLNSRC	HGMD
CLNACC	RCV000080648.4, RCV000177911.1, RCV000177912.2,