rs886043822

Orientation

plus

Stabilized

plus

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

Chromosome

X

Position

32849726

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs886043822
dbSNP (classic)	rs886043822
ClinGen	rs886043822
ebi	rs886043822
HLI	rs886043822
Exac	rs886043822
Gnomad	rs886043822
Varsome	rs886043822
LitVar	rs886043822
Map	rs886043822
PheGenI	rs886043822
Biobank	rs886043822
1000 genomes	rs886043822
hgdp	rs886043822
ensembl	rs886043822
geneview	rs886043822
scholar	rs886043822
google	rs886043822
pharmgkb	rs886043822
gwascentral	rs886043822
openSNP	rs886043822
23andMe	rs886043822
SNPshot	rs886043822
SNPdbe	rs886043822
MSV3d	rs886043822
GWAS Ctlg	rs886043822

Max Magnitude

0

ClinVar
Risk	rs886043822(T;T)
Alt	rs886043822(T;T)
Reference	Rs886043822(A;A)
Significance	Pathogenic
Disease	Becker muscular dystrophy Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Becker muscular dystrophy Duchenne muscular dystrophy
Reversed	0
HGVS	NC_000023.10:g.32867843A>T
CLNSRC
CLNACC	RCV000268267.1, RCV000358417.1,