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rs9333289

From SNPedia

Orientationplus
Stabilizedplus
Make rs9333289(C;C)
Make rs9333289(C;T)
Make rs9333289(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position186633380
GeneITGAV
is asnp
is mentioned by
dbSNPrs9333289
ebirs9333289
HLIrs9333289
Exacrs9333289
Varsomers9333289
Maprs9333289
PheGenIrs9333289
hapmaprs9333289
1000 genomesrs9333289
hgdprs9333289
ensemblrs9333289
gopubmedrs9333289
geneviewrs9333289
scholarrs9333289
googlers9333289
pharmgkbrs9333289
gwascentralrs9333289
openSNPrs9333289
23andMers9333289
23andMe allrs9333289
SNP Nexus

SNPshotrs9333289
SNPdbers9333289
MSV3drs9333289
GWAS Ctlgrs9333289
GMAF0.1827
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

[PMID 14681825OA-icon.png] Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).