rs886042495

Orientation

plus

Stabilized

plus

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

Chromosome

X

Position

31169519

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs886042495
dbSNP (classic)	rs886042495
ClinGen	rs886042495
ebi	rs886042495
HLI	rs886042495
Exac	rs886042495
Gnomad	rs886042495
Varsome	rs886042495
LitVar	rs886042495
Map	rs886042495
PheGenI	rs886042495
Biobank	rs886042495
1000 genomes	rs886042495
hgdp	rs886042495
ensembl	rs886042495
geneview	rs886042495
scholar	rs886042495
google	rs886042495
pharmgkb	rs886042495
gwascentral	rs886042495
openSNP	rs886042495
23andMe	rs886042495
SNPshot	rs886042495
SNPdbe	rs886042495
MSV3d	rs886042495
GWAS Ctlg	rs886042495

Max Magnitude

0

ClinVar
Risk	rs886042495(A;A)
Alt	rs886042495(A;A)
Reference	Rs886042495(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy Becker muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy Becker muscular dystrophy
Reversed	0
HGVS	NC_000023.10:g.31187636G>A
CLNSRC
CLNACC	RCV000294523.1, RCV000345250.1,