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rs886044402

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position32390103
GeneDMD
is asnp
is mentioned by
dbSNPrs886044402
dbSNP (classic)rs886044402
ClinGenrs886044402
ebirs886044402
HLIrs886044402
Exacrs886044402
Gnomadrs886044402
Varsomers886044402
LitVarrs886044402
Maprs886044402
PheGenIrs886044402
Biobankrs886044402
1000 genomesrs886044402
hgdprs886044402
ensemblrs886044402
geneviewrs886044402
scholarrs886044402
googlers886044402
pharmgkbrs886044402
gwascentralrs886044402
openSNPrs886044402
23andMers886044402
SNPshotrs886044402
SNPdbers886044402
MSV3drs886044402
GWAS Ctlgrs886044402
Max Magnitude0
ClinVar
Risk rs886044402(A;A)
Alt rs886044402(A;A)
Reference Rs886044402(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 0
HGVS NC_000023.10:g.32408220G>A
CLNSRC
CLNACC RCV000296982.1,