Gene: TCF4 ×
Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12967143
rs12967143
TCF4
1 1.000 0.040 18 55431781 intron variant G/C snv 0.55 0.700 1.000 2 2018 2019
dbSNP: rs11152363
rs11152363
TCF4
2 1.000 0.040 18 55389957 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11152369
rs11152369
TCF4
5 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs12457157
rs12457157
TCF4
2 1.000 0.040 18 55629696 intron variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs1261070
rs1261070
TCF4
2 1.000 0.040 18 55235854 intron variant A/G snv 0.94 0.700 1.000 1 2018 2018
dbSNP: rs1261114
rs1261114
TCF4
2 1.000 0.040 18 55271138 intron variant G/A snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs12958048
rs12958048
TCF4
1 1.000 0.040 18 55434367 intron variant A/G snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs12963463
rs12963463
TCF4
3 1.000 0.040 18 55431862 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs13381817
rs13381817
TCF4
2 1.000 0.040 18 55230988 non coding transcript exon variant C/T snv 6.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs1452787
rs1452787
TCF4
2 0.827 0.160 18 55539976 intron variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs1452788
rs1452788
TCF4
1 1.000 0.040 18 55450073 intron variant A/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs4801157
rs4801157
TCF4
2 1.000 0.040 18 55497462 intron variant C/T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs599550
rs599550
TCF4
3 1.000 0.040 18 55585157 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs611439
rs611439
TCF4
2 1.000 0.040 18 55537633 intron variant C/T snv 0.94 0.700 1.000 1 2018 2018
dbSNP: rs896686
rs896686
TCF4 ; TCF4-AS1
2 1.000 0.040 18 55455800 intron variant T/G snv 0.12 0.700 1.000 1 2018 2018