Rs104894879

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894879
PheGenIrs104894879
nextbiors104894879
hapmaprs104894879
1000 genomesrs104894879
hgdprs104894879
ensemblrs104894879
gopubmedrs104894879
geneviewrs104894879
scholarrs104894879
googlers104894879
pharmgkbrs104894879
gwascentralrs104894879
openSNPrs104894879
23andMers104894879
23andMe allrs104894879
SNP Nexus

SNPshotrs104894879
SNPdbers104894879
MSV3drs104894879
GeneNDP
ChromosomeX
Orientationminus
Position43958608
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894879(G;G)
Make rs104894879(G;T)
OMIM300658
Desc
Variant0011
Relatedalso
ClinVar
Risk rs104894879(G;G)
Alt rs104894879(G;G)
Reference rs104894879(T;T)
Significance 5
Disease Atrophia bulborum hereditaria
ClinVar info
Gene NDP
CLNDBN Atrophia bulborum hereditaria
Reversed 1
CLNHGVS NC_000023.10:g.43817854A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011435.1