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: rs12978472
rs12978472
INSR
5 19 7257979 intron variant C/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs4247374
rs4247374
INSR
2 19 7252745 intron variant C/T snv 9.7E-02 0.700 1.000 2 2016 2018
dbSNP: rs10427021
rs10427021
INSR
2 19 7259335 intron variant T/C;G snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs11671314
rs11671314
INSR
1 19 7258394 intron variant G/C snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs36047283
rs36047283
INSR
1 19 7255690 intron variant A/G snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs7248104
rs7248104
INSR
2 19 7224420 intron variant G/A snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs75392157
rs75392157
INSR
1 19 7256232 intron variant G/T snv 7.5E-02 0.700 1.000 1 2019 2019