rs886044324

Orientation

plus

Stabilized

plus

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

Chromosome

X

Position

31478375

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs886044324
dbSNP (classic)	rs886044324
ClinGen	rs886044324
ebi	rs886044324
HLI	rs886044324
Exac	rs886044324
Gnomad	rs886044324
Varsome	rs886044324
LitVar	rs886044324
Map	rs886044324
PheGenI	rs886044324
Biobank	rs886044324
1000 genomes	rs886044324
hgdp	rs886044324
ensembl	rs886044324
geneview	rs886044324
scholar	rs886044324
google	rs886044324
pharmgkb	rs886044324
gwascentral	rs886044324
openSNP	rs886044324
23andMe	rs886044324
SNPshot	rs886044324
SNPdbe	rs886044324
MSV3d	rs886044324
GWAS Ctlg	rs886044324

Max Magnitude

0

ClinVar
Risk	rs886044324(G;G)
Alt	rs886044324(G;G)
Reference	Rs886044324(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	0
HGVS	NC_000023.10:g.31496492C>G
CLNSRC
CLNACC	RCV000284523.1,