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rs11902171

From SNPedia

Orientationplus
Stabilizedplus
Make rs11902171(C;C)
Make rs11902171(C;G)
Make rs11902171(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position186678500
GeneITGAV
is asnp
is mentioned by
dbSNPrs11902171
ebirs11902171
HLIrs11902171
Exacrs11902171
Varsomers11902171
Maprs11902171
PheGenIrs11902171
hapmaprs11902171
1000 genomesrs11902171
hgdprs11902171
ensemblrs11902171
gopubmedrs11902171
geneviewrs11902171
scholarrs11902171
googlers11902171
pharmgkbrs11902171
gwascentralrs11902171
openSNPrs11902171
23andMers11902171
23andMe allrs11902171
SNP Nexus

SNPshotrs11902171
SNPdbers11902171
MSV3drs11902171
GWAS Ctlgrs11902171
GMAF0.1653
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 22271436] Single-nucleotide polymorphisms of integrins are associated with the risk and lymph node metastasis of oral squamous cell carcinoma


[PMID 20926544] Allele polymorphisms of tumor integrins correlate with peritoneal carcinosis capability of gastric cancer cells in radically resected patients.


[PMID 23065910] Genetic variants in the integrin gene predicted microRNA-binding sites were associated with the risk of prostate cancer


[PMID 24769516] Polymorphisms of microRNA-Binding Sites in Integrin Genes Are Associated with Oral Squamous Cell Carcinoma Susceptibility and Progression