rs398124038

Orientation

minus

Stabilized

minus

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

Make rs398124038(G;T)

Make rs398124038(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31875343

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124038
dbSNP (classic)	rs398124038
ClinGen	rs398124038
ebi	rs398124038
HLI	rs398124038
Exac	rs398124038
Gnomad	rs398124038
Varsome	rs398124038
LitVar	rs398124038
Map	rs398124038
PheGenI	rs398124038
Biobank	rs398124038
1000 genomes	rs398124038
hgdp	rs398124038
ensembl	rs398124038
geneview	rs398124038
scholar	rs398124038
google	rs398124038
pharmgkb	rs398124038
gwascentral	rs398124038
openSNP	rs398124038
23andMe	rs398124038
SNPshot	rs398124038
SNPdbe	rs398124038
MSV3d	rs398124038
GWAS Ctlg	rs398124038

Max Magnitude

0

ClinVar
Risk	rs398124038(T;T)
Alt	rs398124038(T;T)
Reference	Rs398124038(G;G)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.31893460C>A
CLNSRC	HGMD
CLNACC	RCV000080745.3,