rs398123871

Orientation

minus

Stabilized

minus

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

Make rs398123871(G;T)

Make rs398123871(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32844848

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123871
dbSNP (classic)	rs398123871
ClinGen	rs398123871
ebi	rs398123871
HLI	rs398123871
Exac	rs398123871
Gnomad	rs398123871
Varsome	rs398123871
LitVar	rs398123871
Map	rs398123871
PheGenI	rs398123871
Biobank	rs398123871
1000 genomes	rs398123871
hgdp	rs398123871
ensembl	rs398123871
geneview	rs398123871
scholar	rs398123871
google	rs398123871
pharmgkb	rs398123871
gwascentral	rs398123871
openSNP	rs398123871
23andMe	rs398123871
SNPshot	rs398123871
SNPdbe	rs398123871
MSV3d	rs398123871
GWAS Ctlg	rs398123871

Max Magnitude

0

ClinVar
Risk	rs398123871(T;T)
Alt	rs398123871(T;T)
Reference	Rs398123871(G;G)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32862965C>A
CLNSRC	HGMD
CLNACC	RCV000080475.3,