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: 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
3 0.925 0.080 10 113036289 intron variant A/G snv 0.54 0.700 1.000 1 2007 2007
dbSNP: rs7900150
rs7900150
TCF7L2
3 0.882 0.160 10 113034064 intron variant T/A;C snv 0.54 0.700 1.000 1 2007 2007
dbSNP: rs10885421
rs10885421
TCF7L2
1 1.000 0.080 10 113156827 intron variant G/T snv 0.52 0.010 1.000 1 2018 2018
dbSNP: rs11196175
rs11196175
TCF7L2
2 0.925 0.160 10 112976855 intron variant T/C snv 0.20 0.010 1.000 1 2017 2017
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: rs11196236
rs11196236
TCF7L2
2 0.925 0.160 10 113127963 intron variant T/C snv 0.16 0.010 1.000 1 2009 2009
dbSNP: rs1157868044
rs1157868044
TCF7L2
1 1.000 0.080 10 112951246 missense variant G/A snv 0.010 1.000 1 2015 2015
dbSNP: rs12243326
rs12243326
TCF7L2
5 0.925 0.160 10 113029056 intron variant T/C snv 0.27 0.010 1.000 1 2013 2013
dbSNP: rs1225404
rs1225404
TCF7L2
3 0.882 0.160 10 113154906 intron variant C/T snv 0.71 0.010 1.000 1 2007 2007
dbSNP: rs1427214163
rs1427214163
TCF7L2
2 1.000 0.080 10 113151879 missense variant C/T snv 7.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs148523217
rs148523217
TCF7L2
1 1.000 0.080 10 113146030 missense variant C/A snv 0.010 1.000 1 2008 2008
dbSNP: rs17747324
rs17747324
TCF7L2
4 0.925 0.160 10 112992744 intron variant T/C snv 0.17 0.010 1.000 1 2013 2013
dbSNP: rs290481
rs290481
TCF7L2
9 0.827 0.200 10 113164066 intron variant C/T snv 0.20 0.010 1.000 1 2017 2017
dbSNP: rs4132670
rs4132670
TCF7L2
2 1.000 0.080 10 113008012 intron variant G/A snv 0.39 0.010 1.000 1 2013 2013
dbSNP: rs4918789
rs4918789
TCF7L2
1 1.000 0.080 10 113062048 intron variant T/G snv 0.53 0.010 1.000 1 2008 2008
dbSNP: rs77961654
rs77961654
TCF7L2
1 1.000 0.080 10 113165610 missense variant C/A snv 5.3E-02 2.9E-02 0.010 < 0.001 1 2008 2008
dbSNP: rs7924080
rs7924080
TCF7L2
2 0.925 0.120 10 113027253 intron variant T/C snv 0.55 0.010 1.000 1 2009 2009
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
9 0.763 0.240 10 113014168 intron variant A/G snv 0.55 0.700 1.000 2 2007 2009
dbSNP: rs10885406
rs10885406
TCF7L2
2 0.925 0.120 10 113017965 intron variant A/G snv 0.55 0.020 1.000 2 2008 2009
dbSNP: rs3814573
rs3814573
TCF7L2
2 1.000 0.080 10 113138334 intron variant T/C snv 0.71 0.020 1.000 2 2007 2008
dbSNP: rs10885409
rs10885409
TCF7L2
3 1.000 0.080 10 113048313 intron variant T/C snv 0.54 0.720 1.000 4 2007 2015