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: rs9960767
rs9960767
TCF4
0.925 0.040 18 55487771 intron variant A/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.880 1.000 2 2009 2018
dbSNP: rs17512836
rs17512836
TCF4
0.925 0.040 18 55527730 intron variant T/C snv 2.2E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.810 1.000 1 2011 2014
dbSNP: rs11152369
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013
dbSNP: rs1261117
rs1261117
TCF4
1.000 0.040 18 55282426 intron variant T/C snv 0.11
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2013 2013
dbSNP: rs1452787
rs1452787
TCF4
0.827 0.160 18 55539976 intron variant A/G snv 0.24
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.800 1.000 1 2013 2013
dbSNP: rs17594526
rs17594526
TCF4
1.000 0.040 18 55391007 intron variant C/T snv 6.4E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2009 2009