Gene: INSR ×
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 2019 2019
dbSNP: rs2963
rs2963
INSR
4 0.851 0.240 19 7163143 synonymous variant G/A snv 9.8E-02 0.13 0.010 1.000 1 2010 2010