rs398123893

Orientation

minus

Stabilized

minus

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

Make rs398123893(-;-)

Make rs398123893(-;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32844796

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123893
dbSNP (classic)	rs398123893
ClinGen	rs398123893
ebi	rs398123893
HLI	rs398123893
Exac	rs398123893
Gnomad	rs398123893
Varsome	rs398123893
LitVar	rs398123893
Map	rs398123893
PheGenI	rs398123893
Biobank	rs398123893
1000 genomes	rs398123893
hgdp	rs398123893
ensembl	rs398123893
geneview	rs398123893
scholar	rs398123893
google	rs398123893
pharmgkb	rs398123893
gwascentral	rs398123893
openSNP	rs398123893
23andMe	rs398123893
SNPshot	rs398123893
SNPdbe	rs398123893
MSV3d	rs398123893
GWAS Ctlg	rs398123893

Max Magnitude

0

ClinVar
Risk	rs398123893(-;-)
Alt	rs398123893(-;-)
Reference	Rs398123893(T;T)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32862913delA
CLNSRC	ClinVar
CLNACC	RCV000080506.3,