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: rs7085532
rs7085532
TCF7L2
2 1.000 0.080 10 113099704 intron variant G/A snv 0.72 0.010 1.000 1 2020 2020