Gene: TCF7L2 ×
Source: CURATED ×
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
19 0.554 0.680 10 112998590 intron variant C/G;T snv 0.900 0.953 32 2006 2020
dbSNP: rs7901695
rs7901695
TCF7L2
3 0.851 0.160 10 112994329 intron variant T/C snv 0.34 0.900 1.000 6 2006 2020
dbSNP: rs12255372
rs12255372
TCF7L2
3 0.667 0.480 10 113049143 intron variant G/A;T snv 0.900 0.908 5 2006 2020
dbSNP: rs4506565
rs4506565
TCF7L2
19 0.790 0.280 10 112996282 intron variant A/G;T snv 0.870 0.900 3 2006 2020
dbSNP: rs11196205
rs11196205
TCF7L2
1 0.827 0.200 10 113047288 intron variant G/A;C;T snv 0.800 0.917 0 2006 2020
dbSNP: rs10885409
rs10885409
TCF7L2
3 1.000 0.080 10 113048313 intron variant T/C snv 0.54 0.720 1.000 2 2007 2015
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: rs7904519
rs7904519
TCF7L2
3 0.763 0.240 10 113014168 intron variant A/G snv 0.55 0.700 1.000 2 2007 2009
dbSNP: rs11196192
rs11196192
TCF7L2
1 1.000 0.080 10 113022528 intron variant T/G snv 6.1E-02 0.700 1.000 1 2010 2010
dbSNP: rs386418874
rs386418874
TCF7L2
1 1.000 0.080 10 112988102 intron variant GT/-;GTGT;GTGTGT delins 0.700 1.000 1 2019 2019
dbSNP: rs7100927
rs7100927
TCF7L2
1 0.925 0.080 10 113036289 intron variant A/G snv 0.54 0.700 1.000 1 2007 2007
dbSNP: rs7900150
rs7900150
TCF7L2
1 0.882 0.160 10 113034064 intron variant T/A;C snv 0.54 0.700 1.000 1 2007 2007