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 0.800 1.000 9 2012 2019
dbSNP: rs4506565
rs4506565
TCF7L2
22 0.790 0.280 10 112996282 intron variant A/G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs12243326
rs12243326
TCF7L2
5 0.925 0.160 10 113029056 intron variant T/C snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs12772424
rs12772424
TCF7L2
2 1.000 0.040 10 113120792 intron variant A/T snv 0.57 0.700 1.000 1 2014 2014
dbSNP: rs17747324
rs17747324
TCF7L2
4 0.925 0.160 10 112992744 intron variant T/C snv 0.17 0.700 1.000 1 2015 2015
dbSNP: rs290475
rs290475
TCF7L2
2 1.000 0.040 10 113114260 intron variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs35198068
rs35198068
TCF7L2
2 10 112995025 intron variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs4132670
rs4132670
TCF7L2
2 1.000 0.080 10 113008012 intron variant G/A snv 0.39 0.700 1.000 1 2019 2019