rs398123866

Orientation

minus

Stabilized

minus

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

Make rs398123866(-;-)

Make rs398123866(-;A)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32573608

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123866
dbSNP (classic)	rs398123866
ClinGen	rs398123866
ebi	rs398123866
HLI	rs398123866
Exac	rs398123866
Gnomad	rs398123866
Varsome	rs398123866
LitVar	rs398123866
Map	rs398123866
PheGenI	rs398123866
Biobank	rs398123866
1000 genomes	rs398123866
hgdp	rs398123866
ensembl	rs398123866
geneview	rs398123866
scholar	rs398123866
google	rs398123866
pharmgkb	rs398123866
gwascentral	rs398123866
openSNP	rs398123866
23andMe	rs398123866
SNPshot	rs398123866
SNPdbe	rs398123866
MSV3d	rs398123866
GWAS Ctlg	rs398123866

Max Magnitude

0

ClinVar
Risk	rs398123866(-;-)
Alt	rs398123866(-;-)
Reference	Rs398123866(A;A)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32591725delT
CLNSRC	ClinVar
CLNACC	RCV000080465.3,