rs886043817

Orientation

plus

Stabilized

plus

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

Chromosome

X

Position

31147500

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs886043817
dbSNP (classic)	rs886043817
ClinGen	rs886043817
ebi	rs886043817
HLI	rs886043817
Exac	rs886043817
Gnomad	rs886043817
Varsome	rs886043817
LitVar	rs886043817
Map	rs886043817
PheGenI	rs886043817
Biobank	rs886043817
1000 genomes	rs886043817
hgdp	rs886043817
ensembl	rs886043817
geneview	rs886043817
scholar	rs886043817
google	rs886043817
pharmgkb	rs886043817
gwascentral	rs886043817
openSNP	rs886043817
23andMe	rs886043817
SNPshot	rs886043817
SNPdbe	rs886043817
MSV3d	rs886043817
GWAS Ctlg	rs886043817

Max Magnitude

0

ClinVar
Risk	rs886043817(T;T)
Alt	rs886043817(T;T)
Reference	Rs886043817(A;A)
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.31165617A>T
CLNSRC
CLNACC	RCV000264403.1, RCV000324314.1,