Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7837328
rs7837328
POU5F1B ; CASC8 ; PCAT1
0.882 0.120 8 127410882 intron variant A/G snv 0.52
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.720 1.000 4 2008 2014
dbSNP: rs7837328
rs7837328
POU5F1B ; CASC8 ; PCAT1
0.882 0.120 8 127410882 intron variant A/G snv 0.52
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.720 1.000 3 2008 2015
dbSNP: rs7837328
rs7837328
POU5F1B ; CASC8 ; PCAT1
0.882 0.120 8 127410882 intron variant A/G snv 0.52
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2008 2018
dbSNP: rs7837328
rs7837328
POU5F1B ; CASC8 ; PCAT1
0.882 0.120 8 127410882 intron variant A/G snv 0.52
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.020 1.000 2 2014 2014
dbSNP: rs7837328
rs7837328
POU5F1B ; CASC8 ; PCAT1
0.882 0.120 8 127410882 intron variant A/G snv 0.52
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2008 2018
dbSNP: rs7837328
rs7837328
POU5F1B ; CASC8 ; PCAT1
0.882 0.120 8 127410882 intron variant A/G snv 0.52
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.010 1.000 1 2008 2008
dbSNP: rs7837328
rs7837328
POU5F1B ; CASC8 ; PCAT1
0.882 0.120 8 127410882 intron variant A/G snv 0.52
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2014 2014
dbSNP: rs7837328
rs7837328
POU5F1B ; CASC8 ; PCAT1
0.882 0.120 8 127410882 intron variant A/G snv 0.52
CUI: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2008 2008