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rs1296028

From SNPedia

Orientationplus
Stabilizedplus
Make rs1296028(A;A)
Make rs1296028(A;G)
Make rs1296028(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position11841238
GeneCTSB
is asnp
is mentioned by
dbSNPrs1296028
ebirs1296028
HLIrs1296028
Exacrs1296028
Varsomers1296028
Maprs1296028
PheGenIrs1296028
hapmaprs1296028
1000 genomesrs1296028
hgdprs1296028
ensemblrs1296028
gopubmedrs1296028
geneviewrs1296028
scholarrs1296028
googlers1296028
pharmgkbrs1296028
gwascentralrs1296028
openSNPrs1296028
23andMers1296028
23andMe allrs1296028
SNP Nexus

SNPshotrs1296028
SNPdbers1296028
MSV3drs1296028
GWAS Ctlgrs1296028
GMAF0.1635
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22451204OA-icon.png]
Trait
Title Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
Risk Allele
P-val 0.000001
Odds Ratio 1.1500 None


[PMID 18636124OA-icon.png] Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma.