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rs797046051

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797046051(A;G)
Make rs797046051(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position12531658
GeneTSEN2
is asnp
is mentioned by
dbSNPrs797046051
ebirs797046051
HLIrs797046051
Exacrs797046051
Varsomers797046051
Maprs797046051
PheGenIrs797046051
hapmaprs797046051
1000 genomesrs797046051
hgdprs797046051
ensemblrs797046051
gopubmedrs797046051
geneviewrs797046051
scholarrs797046051
googlers797046051
pharmgkbrs797046051
gwascentralrs797046051
openSNPrs797046051
23andMers797046051
23andMe allrs797046051
SNP Nexus

SNPshotrs797046051
SNPdbers797046051
MSV3drs797046051
GWAS Ctlgrs797046051
Max Magnitude0
ClinVar
Risk rs797046051(G;G)
Alt rs797046051(G;G)
Reference rs797046051(A;A)
Significance Probable-Pathogenic
Disease Pontocerebellar hypoplasia type 2B
Variation info
Gene TSEN2
CLNDBN Pontocerebellar hypoplasia type 2B
Reversed 0
HGVS NC_000003.11:g.12573157A>G
CLNSRC
CLNACC RCV000195073.1,