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rs11685758

From SNPedia

Orientationplus
Stabilizedplus
Make rs11685758(C;C)
Make rs11685758(C;T)
Make rs11685758(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position186668641
GeneITGAV
is asnp
is mentioned by
dbSNPrs11685758
ebirs11685758
HLIrs11685758
Exacrs11685758
Varsomers11685758
Maprs11685758
PheGenIrs11685758
hapmaprs11685758
1000 genomesrs11685758
hgdprs11685758
ensemblrs11685758
gopubmedrs11685758
geneviewrs11685758
scholarrs11685758
googlers11685758
pharmgkbrs11685758
gwascentralrs11685758
openSNPrs11685758
23andMers11685758
23andMe allrs11685758
SNP Nexus

SNPshotrs11685758
SNPdbers11685758
MSV3drs11685758
GWAS Ctlgrs11685758
GMAF0.2511
Max Magnitude
? (C;C) (C;T) (T;T) 28

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