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rs863224168

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224168(C;C)
Make rs863224168(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position55684996
GenePNPT1
is asnp
is mentioned by
dbSNPrs863224168
ebirs863224168
HLIrs863224168
Exacrs863224168
Varsomers863224168
Maprs863224168
PheGenIrs863224168
hapmaprs863224168
1000 genomesrs863224168
hgdprs863224168
ensemblrs863224168
gopubmedrs863224168
geneviewrs863224168
scholarrs863224168
googlers863224168
pharmgkbrs863224168
gwascentralrs863224168
openSNPrs863224168
23andMers863224168
23andMe allrs863224168
SNP Nexus

SNPshotrs863224168
SNPdbers863224168
MSV3drs863224168
GWAS Ctlgrs863224168
Max Magnitude0
ClinVar
Risk rs863224168(C;C)
Alt rs863224168(C;C)
Reference rs863224168(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PNPT1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.55912131A>G
CLNSRC
CLNACC RCV000196562.1,