Source: ALL
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: rs10799667
rs10799667
0.925 0.040 1 20840000 intron variant T/C snv 2.7E-02
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs10799667
rs10799667
0.925 0.040 1 20840000 intron variant T/C snv 2.7E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs143370804
rs143370804
1 21024072 intron variant G/A snv 0.34
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement
0.700 1.000 1 2018 2018
dbSNP: rs17410008
rs17410008
1 20894208 intron variant G/C snv 0.31
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs17449243
rs17449243
1 20847936 non coding transcript exon variant T/C snv 0.10
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2100382
rs2100382
1 20819929 intron variant G/A snv 0.39
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs4654873
rs4654873
1 20825891 intron variant G/A snv 0.29
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs7556221
rs7556221
1 21129066 intron variant C/G snv 0.43
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs75578006
rs75578006
1.000 0.040 1 21019611 intron variant G/A snv 6.2E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs78649275
rs78649275
1.000 0.040 1 21150540 intron variant T/C snv 5.5E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.700 1.000 1 2015 2015