Gene: TCF7L2 ×
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: rs7903146
rs7903146
TCF7L2
16 0.554 0.680 10 112998590 intron variant C/G;T snv 0.900 0.953 28 2006 2020
dbSNP: rs7901695
rs7901695
TCF7L2
2 0.851 0.160 10 112994329 intron variant T/C snv 0.34 0.900 1.000 3 2006 2020
dbSNP: rs4506565
rs4506565
TCF7L2
18 0.790 0.280 10 112996282 intron variant A/G;T snv 0.870 0.900 1 2006 2020
dbSNP: rs34872471
rs34872471
TCF7L2
2 1.000 0.080 10 112994312 intron variant T/C snv 0.29 0.700 1.000 4 2014 2018
dbSNP: rs117229942
rs117229942
TCF7L2
1 1.000 0.080 10 112978018 intron variant C/T snv 5.8E-03 0.700 1.000 2 2018 2019
dbSNP: rs4918796
rs4918796
TCF7L2
2 1.000 0.080 10 113120583 intron variant T/C snv 0.18 0.700 1.000 2 2018 2019
dbSNP: rs386418874
rs386418874
TCF7L2
1 1.000 0.080 10 112988102 intron variant GT/-;GTGT;GTGTGT delins 0.700 1.000 1 2019 2019