rs398123945

Orientation

minus

Stabilized

minus

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

Make rs398123945(-;-)

Make rs398123945(-;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32448495

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123945
dbSNP (classic)	rs398123945
ClinGen	rs398123945
ebi	rs398123945
HLI	rs398123945
Exac	rs398123945
Gnomad	rs398123945
Varsome	rs398123945
LitVar	rs398123945
Map	rs398123945
PheGenI	rs398123945
Biobank	rs398123945
1000 genomes	rs398123945
hgdp	rs398123945
ensembl	rs398123945
geneview	rs398123945
scholar	rs398123945
google	rs398123945
pharmgkb	rs398123945
gwascentral	rs398123945
openSNP	rs398123945
23andMe	rs398123945
SNPshot	rs398123945
SNPdbe	rs398123945
MSV3d	rs398123945
GWAS Ctlg	rs398123945

Max Magnitude

0

ClinVar
Risk	rs398123945(-;-)
Alt	rs398123945(-;-)
Reference	Rs398123945(G;G)
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.32466612delC
CLNSRC	ClinVar
CLNACC	RCV000080594.4, RCV000176743.1, RCV000176744.1,