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: rs121913135
rs121913135
INSR
3 0.882 0.120 19 7125437 missense variant C/A snv 0.010 1.000 1 1993 1993
dbSNP: rs121913147
rs121913147
INSR
2 0.925 0.120 19 7170554 missense variant T/C snv 7.0E-06 0.010 1.000 1 1995 1995
dbSNP: rs1329693158
rs1329693158
INSR
2 0.925 0.120 19 7184454 missense variant C/T snv 4.0E-06 0.010 1.000 1 1995 1995