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rs10174098

From SNPedia

Orientationplus
Stabilizedplus
Make rs10174098(A;A)
Make rs10174098(A;G)
Make rs10174098(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position186628015
GeneITGAV
is asnp
is mentioned by
dbSNPrs10174098
ebirs10174098
HLIrs10174098
Exacrs10174098
Varsomers10174098
Maprs10174098
PheGenIrs10174098
hapmaprs10174098
1000 genomesrs10174098
hgdprs10174098
ensemblrs10174098
gopubmedrs10174098
geneviewrs10174098
scholarrs10174098
googlers10174098
pharmgkbrs10174098
gwascentralrs10174098
openSNPrs10174098
23andMers10174098
23andMe allrs10174098
SNP Nexus

SNPshotrs10174098
SNPdbers10174098
MSV3drs10174098
GWAS Ctlgrs10174098
GMAF0.3586
Max Magnitude
? (A;A) (A;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.