rs115797771
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs115797771(A;A) |
Make rs115797771(A;C) |
Make rs115797771(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 13 |
Position | 73064505 |
Gene | KLF5 |
is a | snp |
is | mentioned by |
dbSNP | rs115797771 |
dbSNP (classic) | rs115797771 |
ClinGen | rs115797771 |
ebi | rs115797771 |
HLI | rs115797771 |
Exac | rs115797771 |
Gnomad | rs115797771 |
Varsome | rs115797771 |
LitVar | rs115797771 |
Map | rs115797771 |
PheGenI | rs115797771 |
Biobank | rs115797771 |
1000 genomes | rs115797771 |
hgdp | rs115797771 |
ensembl | rs115797771 |
geneview | rs115797771 |
scholar | rs115797771 |
rs115797771 | |
pharmgkb | rs115797771 |
gwascentral | rs115797771 |
openSNP | rs115797771 |
23andMe | rs115797771 |
SNPshot | rs115797771 |
SNPdbe | rs115797771 |
MSV3d | rs115797771 |
GWAS Ctlg | rs115797771 |
Max Magnitude | 0 |
[PMID 26315552] Two novel variants on 13q22.1 are associated with risk of esophageal squamous cell carcinoma