Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1076540
rs1076540
22 17957192 intron variant C/T snv 0.21
Serum gamma-glutamyl transferase measurement
0.800 1.000 1 2011 2011
dbSNP: rs11704827
rs11704827
22 17967521 intron variant A/T snv 0.20
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 2 2015 2017
dbSNP: rs10854521
rs10854521
22 17999834 intron variant G/A snv 0.20
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1978968
rs1978968
22 17965347 intron variant C/T snv 0.17
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs1978968
rs1978968
22 17965347 intron variant C/T snv 0.17
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2019 2019
dbSNP: rs1978968
rs1978968
22 17965347 intron variant C/T snv 0.17
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs369081
rs369081
22 17803906 intron variant T/C snv 0.39 0.52
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs450960
rs450960
1.000 0.120 22 17833538 intron variant C/T snv 0.30
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs5992134
rs5992134
22 17951228 intron variant G/T snv 0.26
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs748779
rs748779
22 17842301 non coding transcript exon variant A/G snv 0.51
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs8139817
rs8139817
22 17985603 intron variant A/C snv 0.34
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs9617650
rs9617650
1.000 0.040 22 18006117 non coding transcript exon variant G/C snv 0.19
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9680696
rs9680696
22 17935399 intron variant C/T snv 0.19
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs2277831
rs2277831
0.925 0.040 22 17816431 intron variant A/G snv 0.33
CUI: C0409952
Disease: Idiopathic osteoarthritis
Idiopathic osteoarthritis
Musculoskeletal Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs2277831
rs2277831
0.925 0.040 22 17816431 intron variant A/G snv 0.33
CUI: C1384584
Disease: Generalized osteoarthritis
Generalized osteoarthritis
Musculoskeletal Diseases 0.010 < 0.001 1 2012 2012