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rs104894882

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894882(A;A)
Make rs104894882(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position43949983
GeneNDP
is asnp
is mentioned by
dbSNPrs104894882
ebirs104894882
HLIrs104894882
Exacrs104894882
Varsomers104894882
Maprs104894882
PheGenIrs104894882
hapmaprs104894882
1000 genomesrs104894882
hgdprs104894882
ensemblrs104894882
gopubmedrs104894882
geneviewrs104894882
scholarrs104894882
googlers104894882
pharmgkbrs104894882
gwascentralrs104894882
openSNPrs104894882
23andMers104894882
23andMe allrs104894882
SNP Nexus

SNPshotrs104894882
SNPdbers104894882
MSV3drs104894882
GWAS Ctlgrs104894882
Max Magnitude0
OMIM300658
Desc
Variant0020
Relatedalso
ClinVar
Risk rs104894882(A;A)
Alt rs104894882(A;A)
Reference rs104894882(C;C)
Significance Pathogenic
Disease Atrophia bulborum hereditaria
Variation info
Gene NDP
CLNDBN Atrophia bulborum hereditaria
Reversed 1
HGVS NC_000023.10:g.43809229G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011444.7,