INSR, insulin receptor, 3643

N. diseases: 452; N. variants: 109
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: rs7248104
rs7248104
19 7224420 intron variant G/A snv 0.38
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2013 2018
dbSNP: rs2303672
rs2303672
19 7168394 intron variant T/C snv 4.4E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs4804411
rs4804411
19 7222366 intron variant G/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2019 2019
dbSNP: rs4804416
rs4804416
19 7223837 intron variant T/G snv 0.37
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs62112763
rs62112763
19 7220002 intron variant C/G snv 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018