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rs4742098

From SNPedia

Orientationplus
Stabilizedplus
Make rs4742098(A;A)
Make rs4742098(A;G)
Make rs4742098(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position5470497
GeneCD274, LOC107987045
is asnp
is mentioned by
dbSNPrs4742098
dbSNP (classic)rs4742098
ClinGenrs4742098
ebirs4742098
HLIrs4742098
Exacrs4742098
Gnomadrs4742098
Varsomers4742098
LitVarrs4742098
Maprs4742098
PheGenIrs4742098
Biobankrs4742098
1000 genomesrs4742098
hgdprs4742098
ensemblrs4742098
geneviewrs4742098
scholarrs4742098
googlers4742098
pharmgkbrs4742098
gwascentralrs4742098
openSNPrs4742098
23andMers4742098
SNPshotrs4742098
SNPdbers4742098
MSV3drs4742098
GWAS Ctlgrs4742098
Max Magnitude0

[PMID 28677815OA-icon.png] Variant SNPs at the microRNA complementary site in the B7‑H1 3'‑untranslated region increase the risk of non‑small cell lung cancer.


[PMID 33255938OA-icon.png] SNP-SNP Interaction in Genes Encoding PD-1/PD-L1 Axis as a Potential Risk Factor for Clear Cell Renal Cell Carcinoma.