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rs797045006

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045006(A;A)
Make rs797045006(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position42850904
GeneRNF170
is asnp
is mentioned by
dbSNPrs797045006
ebirs797045006
HLIrs797045006
Exacrs797045006
Varsomers797045006
Maprs797045006
PheGenIrs797045006
hapmaprs797045006
1000 genomesrs797045006
hgdprs797045006
ensemblrs797045006
gopubmedrs797045006
geneviewrs797045006
scholarrs797045006
googlers797045006
pharmgkbrs797045006
gwascentralrs797045006
openSNPrs797045006
23andMers797045006
23andMe allrs797045006
SNP Nexus

SNPshotrs797045006
SNPdbers797045006
MSV3drs797045006
GWAS Ctlgrs797045006
Max Magnitude0
ClinVar
Risk rs797045006(A;A)
Alt rs797045006(A;A)
Reference rs797045006(G;G)
Significance Probable-Pathogenic
Disease Ataxia
Variation info
Gene RNF170
CLNDBN Ataxia, sensory, autosomal dominant
Reversed 1
HGVS NC_000008.10:g.42706047C>T
CLNSRC
CLNACC RCV000190504.2,