INSR, insulin receptor, 3643

N. diseases: 452; N. variants: 109
Disease: Systolic Pressure ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12978472
rs12978472 		19 7257979 intron variant C/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2018 2019
dbSNP: rs4247374
rs4247374 		19 7252745 intron variant C/T snv 9.7E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2016 2018
dbSNP: rs10427021
rs10427021 		19 7259335 intron variant T/C;G snv 0.15
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs11671314
rs11671314 		19 7258394 intron variant G/C snv 0.22
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs36047283
rs36047283 		19 7255690 intron variant A/G snv 0.14
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs7248104
rs7248104 		19 7224420 intron variant G/A snv 0.38
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs75392157
rs75392157 		19 7256232 intron variant G/T snv 7.5E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019