rs398124080

Orientation

minus

Stabilized

minus

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

Make rs398124080(-;-)

Make rs398124080(-;A)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31348594

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124080
dbSNP (classic)	rs398124080
ClinGen	rs398124080
ebi	rs398124080
HLI	rs398124080
Exac	rs398124080
Gnomad	rs398124080
Varsome	rs398124080
LitVar	rs398124080
Map	rs398124080
PheGenI	rs398124080
Biobank	rs398124080
1000 genomes	rs398124080
hgdp	rs398124080
ensembl	rs398124080
geneview	rs398124080
scholar	rs398124080
google	rs398124080
pharmgkb	rs398124080
gwascentral	rs398124080
openSNP	rs398124080
23andMe	rs398124080
SNPshot	rs398124080
SNPdbe	rs398124080
MSV3d	rs398124080
GWAS Ctlg	rs398124080

Max Magnitude

0

ClinVar
Risk	rs398124080(-;-)
Alt	rs398124080(-;-)
Reference	Rs398124080(A;A)
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.31366711delT
CLNSRC	ClinVar
CLNACC	RCV000080821.4, RCV000179587.1, RCV000179588.1,