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rs16902094

From SNPedia

Orientationplus
Stabilizedplus
Make rs16902094(A;A)
Make rs16902094(A;G)
Make rs16902094(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position127308101
GeneLOC101930033
is asnp
is mentioned by
dbSNPrs16902094
ebirs16902094
HLIrs16902094
Exacrs16902094
Varsomers16902094
Maprs16902094
PheGenIrs16902094
hapmaprs16902094
1000 genomesrs16902094
hgdprs16902094
ensemblrs16902094
gopubmedrs16902094
geneviewrs16902094
scholarrs16902094
googlers16902094
pharmgkbrs16902094
gwascentralrs16902094
openSNPrs16902094
23andMers16902094
23andMe allrs16902094
SNP Nexus

SNPshotrs16902094
SNPdbers16902094
MSV3drs16902094
GWAS Ctlgrs16902094
GMAF0.1653
Max Magnitude

[PMID 19767754OA-icon.png] Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility


[PMID 21390317OA-icon.png] Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3.


GET Evidence
rs16902094
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.171875
summary