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rs6029959

From SNPedia

Orientationplus
Stabilizedplus
Make rs6029959(A;A)
Make rs6029959(A;C)
Make rs6029959(C;C)
ReferenceGRCh38 38.1/142
Chromosome20
Position42076024
GeneLOC101927182, PTPRT
is asnp
is mentioned by
dbSNPrs6029959
dbSNP (classic)rs6029959
ClinGenrs6029959
ebirs6029959
HLIrs6029959
Exacrs6029959
Gnomadrs6029959
Varsomers6029959
LitVarrs6029959
Maprs6029959
PheGenIrs6029959
Biobankrs6029959
1000 genomesrs6029959
hgdprs6029959
ensemblrs6029959
geneviewrs6029959
scholarrs6029959
googlers6029959
pharmgkbrs6029959
gwascentralrs6029959
openSNPrs6029959
23andMers6029959
SNPshotrs6029959
SNPdbers6029959
MSV3drs6029959
GWAS Ctlgrs6029959
Max Magnitude0

[PMID 25967969] The Functional Variant in the 3'UTR of PTPRT with the Risk of Esophageal Squamous Cell Carcinoma in a Chinese Population