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rs9909601

From SNPedia

Orientationplus
Stabilizedplus
Make rs9909601(A;A)
Make rs9909601(A;G)
Make rs9909601(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position35490403
GeneE2F3P1
is asnp
is mentioned by
dbSNPrs9909601
ebirs9909601
HLIrs9909601
Exacrs9909601
Varsomers9909601
Maprs9909601
PheGenIrs9909601
hapmaprs9909601
1000 genomesrs9909601
hgdprs9909601
ensemblrs9909601
gopubmedrs9909601
geneviewrs9909601
scholarrs9909601
googlers9909601
pharmgkbrs9909601
gwascentralrs9909601
openSNPrs9909601
23andMers9909601
23andMe allrs9909601
SNP Nexus

SNPshotrs9909601
SNPdbers9909601
MSV3drs9909601
GWAS Ctlgrs9909601
GMAF0.2713
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 23720677OA-icon.png] Genetic variants in pseudogene E2F3P1 confer risk for HBV-related hepatocellular carcinoma in a Chinese population


[PMID 25013402OA-icon.png] A genetic variant in pseudogene E2F3P1 contributes to prognosis of hepatocellular carcinoma