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: rs56232506
rs56232506
TNS3
1.000 0.080 7 47397647 intron variant G/A snv 0.35
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 2 2014 2018
dbSNP: rs12668436
rs12668436
TNS3
7 47509295 intron variant T/C snv 0.23
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs3801081
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs3801081
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs3801081
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs3801081
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2019 2019
dbSNP: rs3801081
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs3801081
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs3801081
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs3801081
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs3801081
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2019 2019
dbSNP: rs56232506
rs56232506
TNS3
1.000 0.080 7 47397647 intron variant G/A snv 0.35
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs59893503
rs59893503
TNS3
7 47397677 intron variant G/A snv 2.6E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs700755
rs700755
TNS3
0.882 0.040 7 47406044 intron variant A/G snv 0.47
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs700755
rs700755
TNS3
0.882 0.040 7 47406044 intron variant A/G snv 0.47
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 1 2019 2019
dbSNP: rs700755
rs700755
TNS3
0.882 0.040 7 47406044 intron variant A/G snv 0.47
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 1 2019 2019
dbSNP: rs73328514
rs73328514
TNS3
1.000 0.120 7 47448971 intron variant A/T snv 0.15
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs7776701
rs7776701
TNS3
0.882 0.040 7 47403036 intron variant T/C snv 0.40
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs7776701
rs7776701
TNS3
0.882 0.040 7 47403036 intron variant T/C snv 0.40
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 1 2016 2016
dbSNP: rs7776701
rs7776701
TNS3
0.882 0.040 7 47403036 intron variant T/C snv 0.40
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs834603
rs834603
TNS3
7 47408324 intron variant A/G snv 0.47
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs834603
rs834603
TNS3
7 47408324 intron variant A/G snv 0.47
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs834603
rs834603
TNS3
7 47408324 intron variant A/G snv 0.47
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs834603
rs834603
TNS3
7 47408324 intron variant A/G snv 0.47
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs865603
rs865603
TNS3
7 47417868 intron variant C/A;G snv
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016