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rs1378897

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1378897(A;A)
Make rs1378897(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position127110414
is asnp
is mentioned by
dbSNPrs1378897
ebirs1378897
HLIrs1378897
Exacrs1378897
Varsomers1378897
Maprs1378897
PheGenIrs1378897
hapmaprs1378897
1000 genomesrs1378897
hgdprs1378897
ensemblrs1378897
gopubmedrs1378897
geneviewrs1378897
scholarrs1378897
googlers1378897
pharmgkbrs1378897
gwascentralrs1378897
openSNPrs1378897
23andMers1378897
23andMe allrs1378897
SNP Nexus

SNPshotrs1378897
SNPdbers1378897
MSV3drs1378897
GWAS Ctlgrs1378897
GMAF0.09091
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 19562729OA-icon.png] Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry