rs151632
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs151632(C;C) |
Make rs151632(C;T) |
Make rs151632(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 3 |
Position | 38302467 |
Gene | SLC22A14 |
is a | snp |
is | mentioned by |
dbSNP | rs151632 |
dbSNP (classic) | rs151632 |
ClinGen | rs151632 |
ebi | rs151632 |
HLI | rs151632 |
Exac | rs151632 |
Gnomad | rs151632 |
Varsome | rs151632 |
LitVar | rs151632 |
Map | rs151632 |
PheGenI | rs151632 |
Biobank | rs151632 |
1000 genomes | rs151632 |
hgdp | rs151632 |
ensembl | rs151632 |
geneview | rs151632 |
scholar | rs151632 |
rs151632 | |
pharmgkb | rs151632 |
gwascentral | rs151632 |
openSNP | rs151632 |
23andMe | rs151632 |
SNPshot | rs151632 |
SNPdbe | rs151632 |
MSV3d | rs151632 |
GWAS Ctlg | rs151632 |
Merged from | Rs1099946 |
GMAF | 0.05601 |
Max Magnitude | 0 |
[PMID 23528102] Association between granzyme B and perforin I polymorphisms and allograft outcomes in Hispanic kidney transplant recipients.