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. Author manuscript; available in PMC: 2021 Feb 1.
Published in final edited form as: Oncogene. 2019 Oct 15;39(6):1246–1259. doi: 10.1038/s41388-019-1061-6

Table 1:

EXO5 SNP frequency in a PCa case-control analysis of data from the Database of Genotypes and Phenotypes.

SNP Chr Base paira Allele 1 AF_Caseb AF_Controlc Allele 2 P-valued OR(95% CI)e
rs3795347 1 40974156 G 0.2388 0.2407 A 0.8808 0.98(0.86-1.13)
rs12068587 1 40974799 A 0.4912 0.3799 G 2.43E-14 1.57(1.40-1.77)
rs11208299 1 40980731 C 0.5009 0.3949 A 4.30E-13 1.53(1.36-1.73)
a

Human genome assembly GRCh37.p13/hg19

b

Allele frequency in PCa patients

c

Allele frequency in healthy controls

d

Chi-square P-value

e

Odds ratio with 95% confidence interval