rs6570507, ADGRG6

N. diseases: 13
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Adolescent idiopathic scoliosis
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
1178 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.810 1.000 3 2013 2018
Scoliosis, unspecified
CUI: C0036439
Disease: Scoliosis, unspecified
135 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.800 1.000 1 2013 2013
Body Height
CUI: C0005890
Disease: Body Height
3972 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 4 2009 2019
Height
CUI: C0489786
Disease: Height
517 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 2 2009 2010
Body Fat Distribution
CUI: C0424621
Disease: Body Fat Distribution
119 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 1 2019 2019
Pulmonary function
CUI: C0231921
Disease: Pulmonary function
259 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 1 2010 2010
Pulmonary function (finding)
CUI: C3160731
Disease: Pulmonary function (finding)
259 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 1 2010 2010
SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1 (finding)
CUI: C2700406
Disease: SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1 (finding)
11 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 1 2013 2013
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
1158 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 1 2018 2018
Smoking
CUI: C0037369
Disease: Smoking
765 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 1 2017 2017
Smoking Behaviors
CUI: C1519383
Disease: Smoking Behaviors
742 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 1 2017 2017
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.030 1.000 3 2015 2018
Multiple Chronic Conditions
CUI: C3266262
Disease: Multiple Chronic Conditions
42 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.010 1.000 1 2018 2018