Source: ALL

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: rs192647746
rs192647746
1.000 0.040 4 181839213 upstream gene variant A/G;T snv
CUI: C0042345
Disease: Varicosity
Varicosity
0.700 1.000 2 2018 2019
dbSNP: rs1028166
rs1028166
0.790 0.080 4 181892145 intron variant G/A snv 0.74
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 1 2014 2014
dbSNP: rs1028166
rs1028166
0.790 0.080 4 181892145 intron variant G/A snv 0.74
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2014 2014
dbSNP: rs1028166
rs1028166
0.790 0.080 4 181892145 intron variant G/A snv 0.74
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2014 2014
dbSNP: rs1028166
rs1028166
0.790 0.080 4 181892145 intron variant G/A snv 0.74
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2014 2014
dbSNP: rs1028166
rs1028166
0.790 0.080 4 181892145 intron variant G/A snv 0.74
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2014 2014
dbSNP: rs1028166
rs1028166
0.790 0.080 4 181892145 intron variant G/A snv 0.74
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2014 2014
dbSNP: rs1028166
rs1028166
0.790 0.080 4 181892145 intron variant G/A snv 0.74
Malignant neoplasm of large intestine
0.700 1.000 1 2014 2014
dbSNP: rs1028166
rs1028166
0.790 0.080 4 181892145 intron variant G/A snv 0.74
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2014 2014
dbSNP: rs1028166
rs1028166
0.790 0.080 4 181892145 intron variant G/A snv 0.74
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs10866247
rs10866247
1.000 0.040 4 181472744 intergenic variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs12510251
rs12510251
1.000 0.040 4 182693431 intron variant G/A snv 0.23
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2015 2015
dbSNP: rs138013532
rs138013532
4 182631880 intron variant C/T snv 5.9E-03
CUI: C0202455
Disease: Platinum measurement
Platinum measurement
0.700 1.000 1 2019 2019
dbSNP: rs1435495
rs1435495
1.000 0.040 4 181472309 intergenic variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs1439283
rs1439283
4 181563616 intergenic variant C/T snv 0.48
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs17071554
rs17071554
1.000 0.040 4 181470082 intergenic variant T/C snv 2.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17072596
rs17072596
1.000 0.080 4 181951296 intron variant C/T snv 0.16
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2008 2008
dbSNP: rs17073715
rs17073715
0.925 0.040 4 182654203 intron variant C/T snv 5.4E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 1.000 1 2018 2018
dbSNP: rs17073715
rs17073715
0.925 0.040 4 182654203 intron variant C/T snv 5.4E-02
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs17198232
rs17198232
1.000 0.040 4 181476832 intergenic variant C/G snv 7.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17198456
rs17198456
1.000 0.040 4 181478812 regulatory region variant G/A snv 5.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs1836655
rs1836655
1.000 0.040 4 181471624 intergenic variant G/A snv 0.68
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs1878468
rs1878468
1.000 0.040 4 181901179 intron variant G/A snv 0.15
CUI: C0024530
Disease: Malaria
Malaria
0.700 1.000 1 2018 2018
dbSNP: rs2309554
rs2309554
4 181902651 intron variant G/A;T snv
CUI: C0085437
Disease: Meningitis, Bacterial
Meningitis, Bacterial
0.700 1.000 1 2019 2019
dbSNP: rs28437883
rs28437883
1.000 0.040 4 181470786 intergenic variant A/G snv 0.20
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017