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rs767608725

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767608725(C;T)
Make rs767608725(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position55643177
GenePNPT1
is asnp
is mentioned by
dbSNPrs767608725
ebirs767608725
HLIrs767608725
Exacrs767608725
Varsomers767608725
Maprs767608725
PheGenIrs767608725
hapmaprs767608725
1000 genomesrs767608725
hgdprs767608725
ensemblrs767608725
gopubmedrs767608725
geneviewrs767608725
scholarrs767608725
googlers767608725
pharmgkbrs767608725
gwascentralrs767608725
openSNPrs767608725
23andMers767608725
23andMe allrs767608725
SNP Nexus

SNPshotrs767608725
SNPdbers767608725
MSV3drs767608725
GWAS Ctlgrs767608725
Max Magnitude0
ClinVar
Risk rs767608725(T;T)
Alt rs767608725(T;T)
Reference rs767608725(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PNPT1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.55870312C>T
CLNSRC
CLNACC RCV000198071.1,