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rs7130881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7130881(A;G)
Make rs7130881(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position69228491
is asnp
is mentioned by
dbSNPrs7130881
ebirs7130881
HLIrs7130881
Exacrs7130881
Varsomers7130881
Maprs7130881
PheGenIrs7130881
hapmaprs7130881
1000 genomesrs7130881
hgdprs7130881
ensemblrs7130881
gopubmedrs7130881
geneviewrs7130881
scholarrs7130881
googlers7130881
pharmgkbrs7130881
gwascentralrs7130881
openSNPrs7130881
23andMers7130881
23andMe allrs7130881
SNP Nexus

SNPshotrs7130881
SNPdbers7130881
MSV3drs7130881
GWAS Ctlgrs7130881
GMAF0.1212
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19767753OA-icon.png]
Trait Prostate cancer
Title Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
Risk Allele G
P-val 8E-13
Odds Ratio NR NR
GWAS snp
PMID [PMID 21743057OA-icon.png]
Trait
Title Genome-wide association study identifies new prostate cancer susceptibility loci.
Risk Allele G
P-val 9E-9
Odds Ratio 1.3100 [1.20-1.44]


GET Evidence
rs7130881
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary