rs398123856

Orientation

minus

Stabilized

minus

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

Make rs398123856(-;AG)

Make rs398123856(AG;AG)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32614442

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123856
dbSNP (classic)	rs398123856
ClinGen	rs398123856
ebi	rs398123856
HLI	rs398123856
Exac	rs398123856
Gnomad	rs398123856
Varsome	rs398123856
LitVar	rs398123856
Map	rs398123856
PheGenI	rs398123856
Biobank	rs398123856
1000 genomes	rs398123856
hgdp	rs398123856
ensembl	rs398123856
geneview	rs398123856
scholar	rs398123856
google	rs398123856
pharmgkb	rs398123856
gwascentral	rs398123856
openSNP	rs398123856
23andMe	rs398123856
SNPshot	rs398123856
SNPdbe	rs398123856
MSV3d	rs398123856
GWAS Ctlg	rs398123856

Max Magnitude

0

ClinVar
Risk	rs398123856(AG;AG)
Alt	rs398123856(AG;AG)
Reference	Rs398123856(-;-)
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.32632560_32632561dupCT
CLNSRC	ClinVar
CLNACC	RCV000080447.3, RCV000174324.1, RCV000174325.1,