rs398124072

Orientation

minus

Stabilized

minus

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

Make rs398124072(C;T)

Make rs398124072(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31496892

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124072
dbSNP (classic)	rs398124072
ClinGen	rs398124072
ebi	rs398124072
HLI	rs398124072
Exac	rs398124072
Gnomad	rs398124072
Varsome	rs398124072
LitVar	rs398124072
Map	rs398124072
PheGenI	rs398124072
Biobank	rs398124072
1000 genomes	rs398124072
hgdp	rs398124072
ensembl	rs398124072
geneview	rs398124072
scholar	rs398124072
google	rs398124072
pharmgkb	rs398124072
gwascentral	rs398124072
openSNP	rs398124072
23andMe	rs398124072
SNPshot	rs398124072
SNPdbe	rs398124072
MSV3d	rs398124072
GWAS Ctlg	rs398124072

Max Magnitude

0

ClinVar
Risk	rs398124072(T;T)
Alt	rs398124072(T;T)
Reference	Rs398124072(C;C)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31515009G>A
CLNSRC	HGMD
CLNACC	RCV000080800.3, RCV000201168.1,