Have questions? Visit https://www.reddit.com/r/SNPedia

rs2290083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 0 common in complete genomics
Make rs2290083(C;C)
Make rs2290083(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position186669014
GeneITGAV
is asnp
is mentioned by
dbSNPrs2290083
ebirs2290083
HLIrs2290083
Exacrs2290083
Varsomers2290083
Maprs2290083
PheGenIrs2290083
hapmaprs2290083
1000 genomesrs2290083
hgdprs2290083
ensemblrs2290083
gopubmedrs2290083
geneviewrs2290083
scholarrs2290083
googlers2290083
pharmgkbrs2290083
gwascentralrs2290083
openSNPrs2290083
23andMers2290083
23andMe allrs2290083
SNP Nexus

SNPshotrs2290083
SNPdbers2290083
MSV3drs2290083
GWAS Ctlgrs2290083
GMAF0.4619
Max Magnitude0

[PMID 18694400] Integrin alpha V polymorphisms and haplotypes in a Korean population are associated with susceptibility to chronic hepatitis and hepatocellular carcinoma