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: rs2284378
rs2284378
RALY
0.851 0.080 20 34000289 intron variant T/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.710 < 0.001 1 2012 2012
dbSNP: rs6059655
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 2 2016 2019
dbSNP: rs6059655
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 2 2016 2019
dbSNP: rs6059655
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 2 2016 2019
dbSNP: rs2284378
rs2284378
RALY
0.851 0.080 20 34000289 intron variant T/C;G snv
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2011 2011
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0346163
Disease: Endometrioid carcinoma ovary
Endometrioid carcinoma ovary 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2016 2016
dbSNP: rs2300206
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs6059655
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs6059655
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2016 2016
dbSNP: rs6059655
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 1.000 1 2016 2016