Gene: TCF7L2 ×
Source: GWASDB ×
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: rs11196174
rs11196174
TCF7L2
1 1.000 0.080 10 112974337 intron variant A/C;G snv 0.800 1.000 1 2013 2013
dbSNP: rs11196175
rs11196175
TCF7L2
1 0.925 0.160 10 112976855 intron variant T/C snv 0.20 0.700 1.000 1 2013 2013