rs398124032

Orientation

minus

Stabilized

minus

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

Make rs398124032(A;A)

Make rs398124032(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32809492

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124032
dbSNP (classic)	rs398124032
ClinGen	rs398124032
ebi	rs398124032
HLI	rs398124032
Exac	rs398124032
Gnomad	rs398124032
Varsome	rs398124032
LitVar	rs398124032
Map	rs398124032
PheGenI	rs398124032
Biobank	rs398124032
1000 genomes	rs398124032
hgdp	rs398124032
ensembl	rs398124032
geneview	rs398124032
scholar	rs398124032
google	rs398124032
pharmgkb	rs398124032
gwascentral	rs398124032
openSNP	rs398124032
23andMe	rs398124032
SNPshot	rs398124032
SNPdbe	rs398124032
MSV3d	rs398124032
GWAS Ctlg	rs398124032

Max Magnitude

0

ClinVar
Risk	rs398124032(A;A) rs398124032(T;T)
Alt	rs398124032(A;A) rs398124032(T;T)
Reference	Rs398124032(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy Dilated cardiomyopathy 3B Becker muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy Dilated cardiomyopathy 3B Becker muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32827609C>A; NC_000023.10:g.32827609C>T
CLNSRC	ClinVar
CLNACC	RCV000316228.1, RCV000080736.4, RCV000179876.1, RCV000179877.1,