rs398123858

Orientation

minus

Stabilized

minus

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

Make rs398123858(A;T)

Make rs398123858(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32849777

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123858
dbSNP (classic)	rs398123858
ClinGen	rs398123858
ebi	rs398123858
HLI	rs398123858
Exac	rs398123858
Gnomad	rs398123858
Varsome	rs398123858
LitVar	rs398123858
Map	rs398123858
PheGenI	rs398123858
Biobank	rs398123858
1000 genomes	rs398123858
hgdp	rs398123858
ensembl	rs398123858
geneview	rs398123858
scholar	rs398123858
google	rs398123858
pharmgkb	rs398123858
gwascentral	rs398123858
openSNP	rs398123858
23andMe	rs398123858
SNPshot	rs398123858
SNPdbe	rs398123858
MSV3d	rs398123858
GWAS Ctlg	rs398123858

Max Magnitude

0

ClinVar
Risk	rs398123858(T;T)
Alt	rs398123858(T;T)
Reference	Rs398123858(A;A)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32867894T>A
CLNSRC	HGMD
CLNACC	RCV000080449.3,