Rs3738919

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dbSNPrs3738919
hapmaprs3738919
hgdprs3738919
ensemblrs3738919
gopubmedrs3738919
scholarrs3738919
googlers3738919
pharmgkbrs3738919
hgvbaseg2prs3738919
medrefsnprs3738919
23andMers3738919
SNP Nexus

GeneITGAV
Chromosome2
Orientationplus
Position187229504
GenotypeEffect
rs3738919(C;C)1.9x risk
rs3738919(A;C)1.9x risk
rs3738919(A;A)common


Genotypes Magnitude Summary
Rs3738919(A;A) 00 common
Rs3738919(A;C) 1.9x risk
Rs3738919(C;C) 1.9x risk

rs3738919, a SNP located in the ITGAV gene, was identified in a European study to be associated with rheumatoid arthritis (RA). [PMID 17615072]

The risk allele for rs3738919 is the more common allele, (C). For the three European Caucasian populations studied (372 RA patients + 330 controls), and combining the (C;C) and (A;C) genotypes in comparison to the (A;A) genotype, the odds ratio for RA = 1.94 (CI: 1.3–2.9, p = 0.002). There was no significant difference in RA risk between those carrying one or two (C) alleles. [PMID 17615072]

An editorial about this finding has been published. [PMID 18001496]

? (A;A) (A;C) (C;C)


[PMID 19818132] The ITGAV rs3738919 variant and susceptibility to rheumatoid arthritis in four Caucasian sample sets