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rs797046006

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797046006(A;G)
Make rs797046006(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66715958
GeneSPTBN2
is asnp
is mentioned by
dbSNPrs797046006
ebirs797046006
HLIrs797046006
Exacrs797046006
Varsomers797046006
Maprs797046006
PheGenIrs797046006
hapmaprs797046006
1000 genomesrs797046006
hgdprs797046006
ensemblrs797046006
gopubmedrs797046006
geneviewrs797046006
scholarrs797046006
googlers797046006
pharmgkbrs797046006
gwascentralrs797046006
openSNPrs797046006
23andMers797046006
23andMe allrs797046006
SNP Nexus

SNPshotrs797046006
SNPdbers797046006
MSV3drs797046006
GWAS Ctlgrs797046006
Max Magnitude0
ClinVar
Risk rs797046006(G;G)
Alt rs797046006(G;G)
Reference rs797046006(A;A)
Significance Probable-Pathogenic
Disease Ataxia
Variation info
Gene SPTBN2
CLNDBN Ataxia
Reversed 1
HGVS NC_000011.9:g.66483429T>C
CLNSRC
CLNACC RCV000192407.1,