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rs146027425

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146027425(C;T)
Make rs146027425(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position47945924
GenePNPO
is asnp
is mentioned by
dbSNPrs146027425
ebirs146027425
HLIrs146027425
Exacrs146027425
Varsomers146027425
Maprs146027425
PheGenIrs146027425
hapmaprs146027425
1000 genomesrs146027425
hgdprs146027425
ensemblrs146027425
gopubmedrs146027425
geneviewrs146027425
scholarrs146027425
googlers146027425
pharmgkbrs146027425
gwascentralrs146027425
openSNPrs146027425
23andMers146027425
23andMe allrs146027425
SNP Nexus

SNPshotrs146027425
SNPdbers146027425
MSV3drs146027425
GWAS Ctlgrs146027425
Max Magnitude0
ClinVar
Risk rs146027425(G,T;G,T)
Alt rs146027425(G,T;G,T)
Reference rs146027425(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PNPO
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.46023290C>T
CLNSRC
CLNACC RCV000188494.2,