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rs2297136

From SNPedia

Orientationminus
Stabilizedminus
Make rs2297136(C;C)
Make rs2297136(C;T)
Make rs2297136(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position5467955
GeneCD274, LOC107987045
is asnp
is mentioned by
dbSNPrs2297136
dbSNP (classic)rs2297136
ClinGenrs2297136
ebirs2297136
HLIrs2297136
Exacrs2297136
Gnomadrs2297136
Varsomers2297136
LitVarrs2297136
Maprs2297136
PheGenIrs2297136
Biobankrs2297136
1000 genomesrs2297136
hgdprs2297136
ensemblrs2297136
geneviewrs2297136
scholarrs2297136
googlers2297136
pharmgkbrs2297136
gwascentralrs2297136
openSNPrs2297136
23andMers2297136
23andMe allrs2297136
SNPshotrs2297136
SNPdbers2297136
MSV3drs2297136
GWAS Ctlgrs2297136
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[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 29940275] Correlations of PD-L1 gene polymorphisms with susceptibility and prognosis in hepatocellular carcinoma in a Chinese Han population.