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: rs61192259
rs61192259
BTBD9
1.000 0.080 6 38486186 intron variant C/A snv 0.50
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.700 1.000 1 2017 2017
dbSNP: rs6458047
rs6458047
BTBD9
1.000 0.040 6 38227184 intron variant A/C snv 0.82
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6917654
rs6917654
BTBD9
1.000 0.040 6 38229263 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs726160
rs726160
BTBD9
1.000 0.040 6 38253863 intron variant A/G snv 0.69
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs7742915
rs7742915
BTBD9
0.790 0.080 6 38179969 intron variant C/T snv 0.64
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2017 2017
dbSNP: rs7742915
rs7742915
BTBD9
0.790 0.080 6 38179969 intron variant C/T snv 0.64
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2017 2017
dbSNP: rs7742915
rs7742915
BTBD9
0.790 0.080 6 38179969 intron variant C/T snv 0.64
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2017 2017
dbSNP: rs7742915
rs7742915
BTBD9
0.790 0.080 6 38179969 intron variant C/T snv 0.64
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2017 2017
dbSNP: rs7742915
rs7742915
BTBD9
0.790 0.080 6 38179969 intron variant C/T snv 0.64
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2017 2017
dbSNP: rs7742915
rs7742915
BTBD9
0.790 0.080 6 38179969 intron variant C/T snv 0.64
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs7742915
rs7742915
BTBD9
0.790 0.080 6 38179969 intron variant C/T snv 0.64
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2017 2017
dbSNP: rs7742915
rs7742915
BTBD9
0.790 0.080 6 38179969 intron variant C/T snv 0.64
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2017 2017
dbSNP: rs7742915
rs7742915
BTBD9
0.790 0.080 6 38179969 intron variant C/T snv 0.64
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2017 2017
dbSNP: rs9296240
rs9296240
BTBD9 ; LOC105375045
1.000 0.040 6 38242743 intron variant G/C snv 0.10
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs9296243
rs9296243
BTBD9
1.000 0.040 6 38279842 intron variant C/G snv 5.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs9349061
rs9349061
BTBD9 ; LOC105375045
1.000 0.040 6 38246669 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs9349063
rs9349063
BTBD9 ; LOC105375045
1.000 0.040 6 38246741 intron variant A/G snv 0.10
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs9462418
rs9462418
BTBD9
1.000 0.040 6 38248669 intron variant C/T snv 0.10
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs72855171
rs72855171
BTBD9
1.000 0.080 6 38604737 intron variant T/C snv 3.0E-02
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2018 2018
dbSNP: rs9369062
rs9369062
BTBD9
6 38469527 intron variant A/C snv 0.25
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2018 2018
dbSNP: rs17757975
rs17757975
BTBD9 ; LOC105375045
6 38246374 intron variant T/C snv 0.12
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs9470875
rs9470875
BTBD9
6 38410432 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019