rs398124106

Orientation

minus

Stabilized

minus

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

Make rs398124106(G;T)

Make rs398124106(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31182850

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124106
dbSNP (classic)	rs398124106
ClinGen	rs398124106
ebi	rs398124106
HLI	rs398124106
Exac	rs398124106
Gnomad	rs398124106
Varsome	rs398124106
LitVar	rs398124106
Map	rs398124106
PheGenI	rs398124106
Biobank	rs398124106
1000 genomes	rs398124106
hgdp	rs398124106
ensembl	rs398124106
geneview	rs398124106
scholar	rs398124106
google	rs398124106
pharmgkb	rs398124106
gwascentral	rs398124106
openSNP	rs398124106
23andMe	rs398124106
SNPshot	rs398124106
SNPdbe	rs398124106
MSV3d	rs398124106
GWAS Ctlg	rs398124106

Max Magnitude

0

ClinVar
Risk	rs398124106(T;T)
Alt	rs398124106(T;T)
Reference	Rs398124106(G;G)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31200967C>A
CLNSRC	HGMD
CLNACC	RCV000080863.4, RCV000179677.1, RCV000179678.1,