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: rs1014290
rs1014290
SLC2A9 ; LOC105374476
0.827 0.280 4 10000237 intron variant G/A snv 0.72
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.800 1.000 2 2010 2019
dbSNP: rs1014290
rs1014290
SLC2A9 ; LOC105374476
0.827 0.280 4 10000237 intron variant G/A snv 0.72
CUI: C0018099
Disease: Gout
Gout 		0.810 1.000 2 2010 2019
dbSNP: rs78154696
rs78154696 		1.000 0.080 5 1000041 upstream gene variant G/A;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs9833888
rs9833888
FILIP1L ; CMSS1
1.000 0.080 3 100004736 intron variant G/T snv 0.18
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs10988944
rs10988944
ERP44
0.925 0.040 9 100011933 intron variant C/A snv 0.20
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs10988944
rs10988944
ERP44
0.925 0.040 9 100011933 intron variant C/A snv 0.20
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs7006527
rs7006527
RGS22
0.851 0.040 8 100012277 intron variant A/C;T snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 2 2014 2015
dbSNP: rs7006527
rs7006527
RGS22
0.851 0.040 8 100012277 intron variant A/C;T snv
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 2 2014 2015
dbSNP: rs7006527
rs7006527
RGS22
0.851 0.040 8 100012277 intron variant A/C;T snv
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 2 2014 2015
dbSNP: rs7323466
rs7323466 		13 100019615 intergenic variant T/C snv 0.64
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs142529006
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs142529006
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs142529006
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs142529006
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs56079856
rs56079856
IDUA
4 1000223 intron variant G/T snv 0.14
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7826222
rs7826222 		1.000 0.080 8 10002570 intron variant G/C snv
CUI: C0028754
Disease: Obesity
Obesity 		0.700 1.000 1 2009 2009
dbSNP: rs1963304
rs1963304
ZKSCAN1
7 100028173 intron variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1015538
rs1015538
ZKSCAN1
7 100028412 intron variant A/G snv 0.72
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs2897075
rs2897075
ZKSCAN1
1.000 0.040 7 100032719 intron variant C/T snv 0.31
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2019 2019
dbSNP: rs10883437
rs10883437 		1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.800 1.000 1 2011 2011
dbSNP: rs10883437
rs10883437 		1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs9585327
rs9585327 		1.000 0.040 13 100037100 intergenic variant G/A snv 0.36
CUI: C0027092
Disease: Myopia
Myopia 		0.700 1.000 1 2016 2016
dbSNP: rs181978376
rs181978376 		10 100037758 downstream gene variant T/A;C snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4486555
rs4486555 		10 100039545 downstream gene variant G/T snv 0.40
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs66803065
rs66803065
SBF2
11 10004305 intron variant C/A;T snv 0.19
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017