Source: BEFREE

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: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.050 1.000 5 2007 2019
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.020 0.500 2 2013 2015
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2016 2016
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		0.010 1.000 1 2014 2014
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0038587
Disease: Substance Withdrawal Syndrome
Substance Withdrawal Syndrome 		0.010 1.000 1 2012 2012
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2016 2016
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2018 2018
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2009 2009
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 2013 2013
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction 		0.010 1.000 1 2011 2011
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2016 2016
dbSNP: rs1881457
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.020 1.000 2 2017 2017
dbSNP: rs1925608
rs1925608
CTNNA3 ; LRRTM3 ; LOC101928961
1.000 0.080 10 66990654 intron variant A/C snv 0.49
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		0.020 0.500 2 2012 2014
dbSNP: rs848
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.020 1.000 2 2008 2011
dbSNP: rs848
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.020 1.000 2 2009 2011
dbSNP: rs151021417
rs151021417
FOXD3 ; FOXD3-AS1
0.925 0.080 1 63323575 missense variant A/C snv 7.2E-05 1.2E-04
CUI: C0003076
Disease: Aniridia
Aniridia 		0.010 1.000 1 2012 2012
dbSNP: rs151021417
rs151021417
FOXD3 ; FOXD3-AS1
0.925 0.080 1 63323575 missense variant A/C snv 7.2E-05 1.2E-04
CUI: C0344559
Disease: Irido-corneo-trabecular dysgenesis (disorder)
Irido-corneo-trabecular dysgenesis (disorder) 		0.010 1.000 1 2012 2012
dbSNP: rs1881457
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2010 2010
dbSNP: rs1881457
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0003467
Disease: Anxiety
Anxiety 		0.010 < 0.001 1 2014 2014
dbSNP: rs1881457
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		0.010 < 0.001 1 2014 2014
dbSNP: rs1881457
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0344315
Disease: Depressed mood
Depressed mood 		0.010 < 0.001 1 2014 2014
dbSNP: rs1881457
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.010 < 0.001 1 2014 2014
dbSNP: rs1881457
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.010 < 0.001 1 2014 2014
dbSNP: rs1881457
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs1881457
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C2747816
Disease: Complicated malaria
Complicated malaria 		0.010 1.000 1 2009 2009