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rs2659051

From SNPedia

Orientationminus
Make rs2659051(C;C)
Make rs2659051(C;G)
Make rs2659051(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position50842312
GeneLOC105372441
is asnp
is mentioned by
dbSNPrs2659051
ebirs2659051
HLIrs2659051
Exacrs2659051
Varsomers2659051
Maprs2659051
PheGenIrs2659051
hapmaprs2659051
1000 genomesrs2659051
hgdprs2659051
ensemblrs2659051
gopubmedrs2659051
geneviewrs2659051
scholarrs2659051
googlers2659051
pharmgkbrs2659051
gwascentralrs2659051
openSNPrs2659051
23andMers2659051
23andMe allrs2659051
SNP Nexus

SNPshotrs2659051
SNPdbers2659051
MSV3drs2659051
GWAS Ctlgrs2659051
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 27409348] Identification and validation of regulatory SNPs that modulate transcription factor chromatin binding and gene expression in prostate cancer.