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: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0346163
Disease: Endometrioid carcinoma ovary
Endometrioid carcinoma ovary 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs11119608
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs12123293
rs12123293
KCNH1 ; LOC105372901
1 210739493 intron variant T/C snv 0.36
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1501562
rs1501562
KCNH1
1.000 0.040 1 210899050 intron variant C/T snv 0.35
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs79589801
rs79589801
KCNH1
1 210880719 intron variant C/T snv 1.2E-02
CUI: C0373705
Disease: Progesterone measurement
Progesterone measurement 		0.700 1.000 1 2019 2019
dbSNP: rs924569
rs924569
KCNH1
1.000 0.040 1 210906276 intron variant T/C snv 0.32
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017