rs398123885

Orientation

minus

Stabilized

minus

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

Make rs398123885(C;C)

Make rs398123885(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32501753

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123885
dbSNP (classic)	rs398123885
ClinGen	rs398123885
ebi	rs398123885
HLI	rs398123885
Exac	rs398123885
Gnomad	rs398123885
Varsome	rs398123885
LitVar	rs398123885
Map	rs398123885
PheGenI	rs398123885
Biobank	rs398123885
1000 genomes	rs398123885
hgdp	rs398123885
ensembl	rs398123885
geneview	rs398123885
scholar	rs398123885
google	rs398123885
pharmgkb	rs398123885
gwascentral	rs398123885
openSNP	rs398123885
23andMe	rs398123885
SNPshot	rs398123885
SNPdbe	rs398123885
MSV3d	rs398123885
GWAS Ctlg	rs398123885

Max Magnitude

0

ClinVar
Risk	rs398123885(C;C)
Alt	rs398123885(C;C)
Reference	Rs398123885(T;T)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32519870A>G
CLNSRC	ClinVar
CLNACC	RCV000080494.3,