Rs104894867

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894867(C;C)
Make rs104894867(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position43949932
GeneNDP
is asnp
is mentioned by
dbSNPrs104894867
Exacrs104894867
PheGenIrs104894867
nextbiors104894867
hapmaprs104894867
1000 genomesrs104894867
hgdprs104894867
ensemblrs104894867
gopubmedrs104894867
geneviewrs104894867
scholarrs104894867
googlers104894867
pharmgkbrs104894867
gwascentralrs104894867
openSNPrs104894867
23andMers104894867
23andMe allrs104894867
SNP Nexus

SNPshotrs104894867
SNPdbers104894867
MSV3drs104894867
OMIM300658
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894867(C;C)
Alt rs104894867(C;C)
Reference rs104894867(G;G)
Significance Pathogenic
Disease Atrophia bulborum hereditaria
Variation info
Gene NDP
CLNDBN Atrophia bulborum hereditaria
Reversed 1
HGVS NC_000023.10:g.43809178C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011425.6,