rs886043428

Orientation

plus

Stabilized

plus

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

Chromosome

X

Position

32287596

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs886043428
dbSNP (classic)	rs886043428
ClinGen	rs886043428
ebi	rs886043428
HLI	rs886043428
Exac	rs886043428
Gnomad	rs886043428
Varsome	rs886043428
LitVar	rs886043428
Map	rs886043428
PheGenI	rs886043428
Biobank	rs886043428
1000 genomes	rs886043428
hgdp	rs886043428
ensembl	rs886043428
geneview	rs886043428
scholar	rs886043428
google	rs886043428
pharmgkb	rs886043428
gwascentral	rs886043428
openSNP	rs886043428
23andMe	rs886043428
SNPshot	rs886043428
SNPdbe	rs886043428
MSV3d	rs886043428
GWAS Ctlg	rs886043428

Max Magnitude

0

ClinVar
Risk	rs886043428(A;A)
Alt	rs886043428(A;A)
Reference	Rs886043428(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	0
HGVS	NC_000023.10:g.32305713G>A
CLNSRC
CLNACC	RCV000272431.1,