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: rs2291725
rs2291725
GIP
4 0.882 0.120 17 48961770 missense variant T/C snv 0.50 0.40 0.010 1.000 1 2010 2010
dbSNP: rs2291726
rs2291726
GIP
3 0.925 0.080 17 48961892 intron variant T/A;C snv 0.010 1.000 1 2010 2010
dbSNP: rs937301
rs937301
GIP
1 1.000 0.080 17 48968914 upstream gene variant A/G snv 0.55 0.010 1.000 1 2010 2010