rs4742098
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4742098(A;A) |
Make rs4742098(A;G) |
Make rs4742098(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 5470497 |
Gene | CD274, LOC107987045 |
is a | snp |
is | mentioned by |
dbSNP | rs4742098 |
dbSNP (classic) | rs4742098 |
ClinGen | rs4742098 |
ebi | rs4742098 |
HLI | rs4742098 |
Exac | rs4742098 |
Gnomad | rs4742098 |
Varsome | rs4742098 |
LitVar | rs4742098 |
Map | rs4742098 |
PheGenI | rs4742098 |
Biobank | rs4742098 |
1000 genomes | rs4742098 |
hgdp | rs4742098 |
ensembl | rs4742098 |
geneview | rs4742098 |
scholar | rs4742098 |
rs4742098 | |
pharmgkb | rs4742098 |
gwascentral | rs4742098 |
openSNP | rs4742098 |
23andMe | rs4742098 |
SNPshot | rs4742098 |
SNPdbe | rs4742098 |
MSV3d | rs4742098 |
GWAS Ctlg | rs4742098 |
Max Magnitude | 0 |
[PMID 28677815] Variant SNPs at the microRNA complementary site in the B7‑H1 3'‑untranslated region increase the risk of non‑small cell lung cancer.
[PMID 33255938] SNP-SNP Interaction in Genes Encoding PD-1/PD-L1 Axis as a Potential Risk Factor for Clear Cell Renal Cell Carcinoma.