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: rs11706832
rs11706832 		1.000 0.040 3 66452557 intron variant A/C;G snv
CUI: C0017638
Disease: Glioma
Glioma 		Neoplasms 0.710 1.000 2 2017 2018
dbSNP: rs11706832
rs11706832 		1.000 0.040 3 66452557 intron variant A/C;G snv
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		Neoplasms; Nervous System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs9827908
rs9827908 		1.000 3 66395177 intron variant A/G snv 5.2E-02
CUI: C0442874
Disease: Neuropathy
Neuropathy 		Nervous System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs202007714
rs202007714 		1.000 0.040 3 66383098 missense variant G/A;C snv 1.4E-04; 4.0E-06
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2018 2018
dbSNP: rs3965156
rs3965156 		3 66434532 intron variant A/C;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs2306272
rs2306272 		1.000 0.080 3 66384219 missense variant T/C snv 0.31 0.25
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs34080181
rs34080181 		1.000 0.080 3 66403767 intron variant G/A;C snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018