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Rs104894875

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894875
PheGenIrs104894875
hapmaprs104894875
1000 genomesrs104894875
hgdprs104894875
ensemblrs104894875
gopubmedrs104894875
geneviewrs104894875
scholarrs104894875
googlers104894875
pharmgkbrs104894875
gwascentralrs104894875
openSNPrs104894875
23andMers104894875
23andMe allrs104894875
SNP Nexus

SNPshotrs104894875
SNPdbers104894875
MSV3drs104894875
GeneNDP
ChromosomeX
Orientationminus
Position43949888
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894875(A;A)
Make rs104894875(A;G)
OMIM300658
Desc
Variant0015
Relatedalso
ClinVar
Risk rs104894875(A;A)
Alt rs104894875(A;A)
Reference rs104894875(G;G)
Significance 5
Disease Atrophia bulborum hereditaria
ClinVar info
Gene NDP
CLNDBN Atrophia bulborum hereditaria
Reversed 1
CLNHGVS NC_000023.10:g.43809134C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011439.3