Source: GWASCAT

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: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.900 0.945 14 2007 2019
dbSNP: rs10505477
rs10505477
POU5F1B ; CASC8 ; PCAT1
0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.890 0.938 4 2007 2019
dbSNP: rs7014346
rs7014346
POU5F1B ; CASC8 ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.830 0.889 3 2008 2019
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.800 0.871 8 2007 2019
dbSNP: rs16901979
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.800 0.955 5 2007 2019
dbSNP: rs13281615
rs13281615
POU5F1B ; CASC8 ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.800 0.864 4 2007 2017
dbSNP: rs2466035
rs2466035
PCAT1 ; CASC19
0.925 0.120 8 127198984 intron variant T/C snv 0.43
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.800 1.000 1 2013 2013
dbSNP: rs6983561
rs6983561
PCAT1 ; CASC19
0.925 0.080 8 127094635 intron variant A/C snv 0.17
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.780 1.000 2 2008 2017
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.770 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		0.760 0.857 1 2010 2019
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.730 1.000 14 2007 2019
dbSNP: rs1562430
rs1562430
POU5F1B ; CASC8 ; PCAT1 ; CASC21
0.807 0.160 8 127375606 intron variant T/C snv 0.41
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.730 1.000 2 2010 2015
dbSNP: rs1456315
rs1456315
PCAT1 ; PRNCR1 ; CASC19
0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.720 1.000 2 2010 2014
dbSNP: rs13254738
rs13254738
PCAT1 ; PRNCR1 ; CASC19
0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.720 0.667 1 2008 2012
dbSNP: rs16902094
rs16902094
CASC8 ; PCAT1 ; CASC21
0.882 0.160 8 127308101 intron variant A/G snv 0.15
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.720 1.000 1 2009 2017
dbSNP: rs188140481
rs188140481
PCAT1 ; CASC19
0.925 0.080 8 127179427 non coding transcript exon variant T/A;C snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.720 1.000 1 2012 2015
dbSNP: rs116041037
rs116041037
PCAT1 ; CASC19
0.925 0.080 8 127119564 intron variant G/A snv 1.0E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.710 1.000 1 2015 2015
dbSNP: rs7013278
rs7013278
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.776 0.080 8 127402647 intron variant T/C snv 0.59
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.710 1.000 1 2012 2019
dbSNP: rs72725854
rs72725854
PCAT1
0.925 0.080 8 127062570 intron variant A/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.710 1.000 1 2018 2018
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 14 2007 2019