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rs3911238

From SNPedia

Orientationminus
Stabilizedminus
Make rs3911238(C;C)
Make rs3911238(C;G)
Make rs3911238(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position186605617
GeneITGAV
is asnp
is mentioned by
dbSNPrs3911238
ebirs3911238
HLIrs3911238
Exacrs3911238
Varsomers3911238
Maprs3911238
PheGenIrs3911238
hapmaprs3911238
1000 genomesrs3911238
hgdprs3911238
ensemblrs3911238
gopubmedrs3911238
geneviewrs3911238
scholarrs3911238
googlers3911238
pharmgkbrs3911238
gwascentralrs3911238
openSNPrs3911238
23andMers3911238
23andMe allrs3911238
SNP Nexus

SNPshotrs3911238
SNPdbers3911238
MSV3drs3911238
GWAS Ctlgrs3911238
GMAF0.3522
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 19818132OA-icon.png] The ITGAV rs3738919 variant and susceptibility to rheumatoid arthritis in four Caucasian sample sets


[PMID 21116829] A polymorphism in the integrin alphaV subunit gene affects the progression of primary biliary cirrhosis in Japanese patients.