IRS2, insulin receptor substrate 2, 8660

N. diseases: 18; N. variants: 3
Source: CURATED ×
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: rs754205
rs754205 		13 109759295 intron variant A/C;G snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs754205
rs754205 		13 109759295 intron variant A/C;G snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs754205
rs754205 		13 109759295 intron variant A/C;G snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs754205
rs754205 		13 109759295 intron variant A/C;G snv
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs137852740
rs137852740 		1.000 0.080 13 109784115 missense variant G/A;C snv 2.2E-05; 9.3E-05
CUI: C4016690
Disease: DIABETES, TYPE II, SUSCEPTIBILITY TO
DIABETES, TYPE II, SUSCEPTIBILITY TO 		0.700 0
dbSNP: rs1805097
rs1805097 		0.689 0.360 13 109782884 missense variant C/G;T snv 0.35
CUI: C4016690
Disease: DIABETES, TYPE II, SUSCEPTIBILITY TO
DIABETES, TYPE II, SUSCEPTIBILITY TO 		0.700 0