rs398123854

Orientation

minus

Stabilized

minus

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

Make rs398123854(-;G)

Make rs398123854(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32644156

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123854
dbSNP (classic)	rs398123854
ClinGen	rs398123854
ebi	rs398123854
HLI	rs398123854
Exac	rs398123854
Gnomad	rs398123854
Varsome	rs398123854
LitVar	rs398123854
Map	rs398123854
PheGenI	rs398123854
Biobank	rs398123854
1000 genomes	rs398123854
hgdp	rs398123854
ensembl	rs398123854
geneview	rs398123854
scholar	rs398123854
google	rs398123854
pharmgkb	rs398123854
gwascentral	rs398123854
openSNP	rs398123854
23andMe	rs398123854
SNPshot	rs398123854
SNPdbe	rs398123854
MSV3d	rs398123854
GWAS Ctlg	rs398123854

Max Magnitude

0

ClinVar
Risk	rs398123854(G;G)
Alt	rs398123854(G;G)
Reference	Rs398123854(-;-)
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.32662274dupC
CLNSRC	ClinVar
CLNACC	RCV000080441.3, RCV000174092.1, RCV000174093.1,