Rs104894789

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894789(C;T)
Make rs104894789(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31182784
GeneDMD
is asnp
is mentioned by
dbSNPrs104894789
PheGenIrs104894789
nextbiors104894789
hapmaprs104894789
1000 genomesrs104894789
hgdprs104894789
ensemblrs104894789
gopubmedrs104894789
geneviewrs104894789
scholarrs104894789
googlers104894789
pharmgkbrs104894789
gwascentralrs104894789
openSNPrs104894789
23andMers104894789
23andMe allrs104894789
SNP Nexus

SNPshotrs104894789
SNPdbers104894789
MSV3drs104894789
Max Magnitude0
OMIM300377
Desc
Variant0036
Relatedalso
ClinVar
Risk rs104894789(T;T)
Alt rs104894789(T;T)
Reference rs104894789(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31200901G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011993.1,