Gene: TCF7L2 ×
Source: ALL
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
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.090 0.444 9 2007 2017
dbSNP: rs11196236
rs11196236
TCF7L2
2 0.925 0.160 10 113127963 intron variant T/C snv 0.16 0.030 0.333 3 2009 2013
dbSNP: rs12255372
rs12255372
TCF7L2
28 0.667 0.480 10 113049143 intron variant G/A;T snv 0.030 1.000 3 2014 2015
dbSNP: rs11196218
rs11196218
TCF7L2
2 0.925 0.160 10 113080735 intron variant G/A snv 0.25 0.020 < 0.001 2 2010 2012
dbSNP: rs12243326
rs12243326
TCF7L2
5 0.925 0.160 10 113029056 intron variant T/C snv 0.27 0.020 1.000 2 2014 2015
dbSNP: rs290487
rs290487
TCF7L2
10 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.020 0.500 2 2010 2012
dbSNP: rs11196229
rs11196229
TCF7L2
2 0.925 0.160 10 113106413 intron variant G/A snv 0.19 0.010 1.000 1 2009 2009
dbSNP: rs4506565
rs4506565
TCF7L2
22 0.790 0.280 10 112996282 intron variant A/G;T snv 0.010 1.000 1 2014 2014