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rs151166046

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151166046(A;A)
Make rs151166046(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position55680879
GenePNPT1
is asnp
is mentioned by
dbSNPrs151166046
ebirs151166046
HLIrs151166046
Exacrs151166046
Varsomers151166046
Maprs151166046
PheGenIrs151166046
hapmaprs151166046
1000 genomesrs151166046
hgdprs151166046
ensemblrs151166046
gopubmedrs151166046
geneviewrs151166046
scholarrs151166046
googlers151166046
pharmgkbrs151166046
gwascentralrs151166046
openSNPrs151166046
23andMers151166046
23andMe allrs151166046
SNP Nexus

SNPshotrs151166046
SNPdbers151166046
MSV3drs151166046
GWAS Ctlgrs151166046
Max Magnitude0
ClinVar
Risk rs151166046(A;A)
Alt rs151166046(A;A)
Reference rs151166046(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PNPT1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.55908014G>A
CLNSRC
CLNACC RCV000199028.2,