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: rs10166942
rs10166942 		0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.870 1.000 10 2011 2019
dbSNP: rs6741751
rs6741751 		0.925 0.040 2 233919016 intron variant G/A snv 7.8E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.800 1.000 1 2013 2013
dbSNP: rs10166942
rs10166942 		0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40
CUI: C0338480
Disease: Common Migraine
Common Migraine 		Nervous System Diseases 0.710 1.000 2 2013 2019
dbSNP: rs10490012
rs10490012 		2 233934849 intron variant C/T snv 0.34
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2019 2019
dbSNP: rs17862920
rs17862920 		2 233919350 intron variant C/T snv 9.7E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1965629
rs1965629 		2 233916086 upstream gene variant A/G snv 0.40
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2362290
rs2362290 		2 233916724 upstream gene variant G/A snv 0.40
CUI: C0018681
Disease: Headache
Headache 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2018 2018
dbSNP: rs6741751
rs6741751 		0.925 0.040 2 233919016 intron variant G/A snv 7.8E-02
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura 		Nervous System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs6741751
rs6741751 		0.925 0.040 2 233919016 intron variant G/A snv 7.8E-02
CUI: C0338480
Disease: Common Migraine
Common Migraine 		Nervous System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10166942
rs10166942 		0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura 		Nervous System Diseases 0.020 1.000 2 2015 2019
dbSNP: rs10166942
rs10166942 		0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2012 2012
dbSNP: rs10803666
rs10803666 		1.000 0.120 2 233930302 intron variant G/C snv 0.11
CUI: C0264423
Disease: Asthma, Occupational
Asthma, Occupational 		Respiratory Tract Diseases; Immune System Diseases; Occupational Diseases 0.010 1.000 1 2017 2017
dbSNP: rs11562975
rs11562975 		1.000 0.080 2 233945906 synonymous variant G/C snv 0.13 9.2E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs12472151
rs12472151 		1.000 0.040 2 233944048 intron variant G/A snv 4.2E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015