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: rs290481
rs290481
TCF7L2
9 0.827 0.200 10 113164066 intron variant C/T snv 0.20 0.010 1.000 1 2013 2013
dbSNP: rs290487
rs290487
TCF7L2
10 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2013 2013
dbSNP: rs290489
rs290489
TCF7L2
1 1.000 0.080 10 113147296 intron variant A/G snv 0.27 0.010 1.000 1 2013 2013