Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2523722
rs2523722
TRIM26
1.000 0.040 6 30197496 intron variant C/T snv 0.23
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 2 2012 2013
dbSNP: rs2021722
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2011 2013
dbSNP: rs2021722
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013
dbSNP: rs4711211
rs4711211
TRIM26
1.000 0.120 6 30195032 intron variant A/G snv 0.17
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 2 2007 2009
dbSNP: rs11967808
rs11967808
TRIM26
1.000 0.040 6 30211411 intron variant G/C snv 3.2E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs2072107
rs2072107
TRIM26
1.000 6 30199158 splice region variant G/A snv 0.12
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs2072107
rs2072107
TRIM26
1.000 6 30199158 splice region variant G/A snv 0.12
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2010 2010
dbSNP: rs2072107
rs2072107
TRIM26
1.000 6 30199158 splice region variant G/A snv 0.12
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2072107
rs2072107
TRIM26
1.000 6 30199158 splice region variant G/A snv 0.12
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2844775
rs2844775
TRIM26
6 30211645 intron variant G/A snv 0.19
CUI: C0002957
Disease: Anger
Anger 		0.700 1.000 1 2014 2014