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: rs7309
rs7309 		2 161236129 3 prime UTR variant G/A snv 0.42
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2017 2019
dbSNP: rs10930013
rs10930013 		1.000 0.040 2 161213814 intron variant G/A snv 0.43
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs10930013
rs10930013 		1.000 0.040 2 161213814 intron variant G/A snv 0.43
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs11884495
rs11884495 		2 161203458 intron variant A/T snv 0.48 0.43
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs1267068
rs1267068 		2 161155624 intron variant T/G snv 0.26
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs3754970
rs3754970 		2 161235325 intron variant T/A;C;G snv 2.7E-05; 0.48
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs7568498
rs7568498 		1.000 2 161172602 intron variant T/G snv 0.11
CUI: C0442874
Disease: Neuropathy
Neuropathy 		Nervous System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs7568498
rs7568498 		1.000 2 161172602 intron variant T/G snv 0.11
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2014 2014
dbSNP: rs7568498
rs7568498 		1.000 2 161172602 intron variant T/G snv 0.11
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2014 2014
dbSNP: rs7568498
rs7568498 		1.000 2 161172602 intron variant T/G snv 0.11
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2014 2014
dbSNP: rs7568498
rs7568498 		1.000 2 161172602 intron variant T/G snv 0.11
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2014 2014
dbSNP: rs1921310
rs1921310 		1.000 0.120 2 161192690 intron variant A/G snv 0.15
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs3820998
rs3820998 		0.882 0.120 2 161138615 intron variant C/A;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2012 2012
dbSNP: rs3820998
rs3820998 		0.882 0.120 2 161138615 intron variant C/A;T snv
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3820998
rs3820998 		0.882 0.120 2 161138615 intron variant C/A;T snv
CUI: C0085605
Disease: Liver Failure
Liver Failure 		Digestive System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3835942
rs3835942 		1.000 0.040 2 161226860 intron variant -/GGTAATAAACAACCATGAGGTCTTTTTCTTTTGTCAATATACAACGTGATTATACTGAGAAG delins
CUI: C0206368
Disease: Exfoliation Syndrome
Exfoliation Syndrome 		Eye Diseases 0.010 1.000 1 2019 2019