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rs6470517

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs6470517(A;G)
Make rs6470517(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position127448159
GeneFUNDC2P2
is asnp
is mentioned by
dbSNPrs6470517
ebirs6470517
HLIrs6470517
Exacrs6470517
Varsomers6470517
Maprs6470517
PheGenIrs6470517
hapmaprs6470517
1000 genomesrs6470517
hgdprs6470517
ensemblrs6470517
gopubmedrs6470517
geneviewrs6470517
scholarrs6470517
googlers6470517
pharmgkbrs6470517
gwascentralrs6470517
openSNPrs6470517
23andMers6470517
23andMe allrs6470517
SNP Nexus

SNPshotrs6470517
SNPdbers6470517
MSV3drs6470517
GWAS Ctlgrs6470517
GMAF0.1217
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