rs6029959
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6029959(A;A) |
Make rs6029959(A;C) |
Make rs6029959(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 20 |
Position | 42076024 |
Gene | LOC101927182, PTPRT |
is a | snp |
is | mentioned by |
dbSNP | rs6029959 |
dbSNP (classic) | rs6029959 |
ClinGen | rs6029959 |
ebi | rs6029959 |
HLI | rs6029959 |
Exac | rs6029959 |
Gnomad | rs6029959 |
Varsome | rs6029959 |
LitVar | rs6029959 |
Map | rs6029959 |
PheGenI | rs6029959 |
Biobank | rs6029959 |
1000 genomes | rs6029959 |
hgdp | rs6029959 |
ensembl | rs6029959 |
geneview | rs6029959 |
scholar | rs6029959 |
rs6029959 | |
pharmgkb | rs6029959 |
gwascentral | rs6029959 |
openSNP | rs6029959 |
23andMe | rs6029959 |
SNPshot | rs6029959 |
SNPdbe | rs6029959 |
MSV3d | rs6029959 |
GWAS Ctlg | rs6029959 |
Max Magnitude | 0 |
[PMID 25967969] The Functional Variant in the 3'UTR of PTPRT with the Risk of Esophageal Squamous Cell Carcinoma in a Chinese Population