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: rs4513093
rs4513093
0.882 0.200 16 82872937 intron variant A/C;G snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 1.000 1 2018 2018
dbSNP: rs4782534
rs4782534
1.000 0.040 16 83423407 intron variant G/A;C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs61527214
rs61527214
16 83574994 intron variant G/A snv 0.36
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs7193703
rs7193703
1.000 0.040 16 83624538 intron variant A/G snv 9.9E-03
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.700 1.000 1 2016 2016
dbSNP: rs7196583
rs7196583
16 83111245 intron variant T/A;C;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs7206608
rs7206608
16 82839023 intron variant C/G snv 0.32
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs7500448
rs7500448
1.000 0.040 16 83012185 intron variant A/G snv 0.20
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs77347308
rs77347308
1.000 0.040 16 82761814 intron variant A/G;T snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.700 1.000 1 2016 2016
dbSNP: rs77894924
rs77894924
1.000 0.080 16 83521415 intron variant G/A;T snv 6.7E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2016 2016
dbSNP: rs8056960
rs8056960
16 83357533 intron variant C/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9933476
rs9933476
16 83353192 intron variant G/A snv 0.57
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018