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: rs891088
rs891088
19 7184751 intron variant A/G snv 0.32
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 2 2010 2014
dbSNP: rs10421414
rs10421414
19 7133924 intron variant T/C snv 0.19
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs34840745
rs34840745
19 7183786 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs4804413
rs4804413
19 7222644 intron variant C/T snv 0.37
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019