rs972936, IGF1;LINC02456

N. diseases: 12
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.
Forced expiratory volume function
CUI: C0016529
Disease: Forced expiratory volume function
1169 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.700 1.000 1 2019 2019
peak expiratory flow (procedure)
CUI: C1518922
Disease: peak expiratory flow (procedure)
119 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.700 1.000 1 2019 2019
Vital capacity
CUI: C0042834
Disease: Vital capacity
746 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.700 1.000 1 2019 2019
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1.000 1 2012 2012
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1.000 1 2012 2012
Behavioral and psychological symptoms of dementia
CUI: C4285807
Disease: Behavioral and psychological symptoms of dementia
9 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1.000 1 2019 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1.000 1 2015 2015
Dizziness
CUI: C0012833
Disease: Dizziness
14 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1.000 1 2019 2019
Mild cognitive disorder
CUI: C1270972
Disease: Mild cognitive disorder
96 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1.000 1 2015 2015
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1 2015 2015
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1.000 1 2017 2017
Vertigo
CUI: C0042571
Disease: Vertigo
35 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1.000 1 2019 2019