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: rs1035941
rs1035941
INSR
1 19 7199928 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1035942
rs1035942
INSR
3 0.925 0.120 19 7199792 intron variant A/G snv 0.75 0.700 1.000 1 2013 2013
dbSNP: rs10405423
rs10405423
INSR
1 19 7211300 intron variant C/A;G snv 0.700 1.000 1 2019 2019