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rs7789197

From SNPedia

Orientationplus
Stabilizedplus
Make rs7789197(A;A)
Make rs7789197(A;G)
Make rs7789197(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position40925528
is asnp
is mentioned by
dbSNPrs7789197
ebirs7789197
HLIrs7789197
Exacrs7789197
Varsomers7789197
Maprs7789197
PheGenIrs7789197
hapmaprs7789197
1000 genomesrs7789197
hgdprs7789197
ensemblrs7789197
gopubmedrs7789197
geneviewrs7789197
scholarrs7789197
googlers7789197
pharmgkbrs7789197
gwascentralrs7789197
openSNPrs7789197
23andMers7789197
23andMe allrs7789197
SNP Nexus

SNPshotrs7789197
SNPdbers7789197
MSV3drs7789197
GWAS Ctlgrs7789197
GMAF0.2916
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22219177OA-icon.png]
Trait
Title A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants.
Risk Allele
P-val 0.000003
Odds Ratio 1.5152 None