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: rs3769050
rs3769050
0.925 0.040 2 237861037 intron variant A/G;T snv
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs3769050
rs3769050
0.925 0.040 2 237861037 intron variant A/G;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs10199956
rs10199956
1.000 0.040 2 237907946 intron variant T/A;G snv
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3754701
rs3754701
0.882 0.120 2 237858561 upstream gene variant A/C;T snv
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
Nervous System Diseases 0.010 < 0.001 1 2013 2013
dbSNP: rs3754701
rs3754701
0.882 0.120 2 237858561 upstream gene variant A/C;T snv
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs3754701
rs3754701
0.882 0.120 2 237858561 upstream gene variant A/C;T snv
CUI: C0338480
Disease: Common Migraine
Common Migraine
Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3754701
rs3754701
0.882 0.120 2 237858561 upstream gene variant A/C;T snv
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3769048
rs3769048
0.925 0.120 2 237861218 intron variant G/A snv 2.2E-02
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs3769048
rs3769048
0.925 0.120 2 237861218 intron variant G/A snv 2.2E-02
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2017 2017