IRS2, insulin receptor substrate 2, 8660

N. diseases: 152; N. variants: 6
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: rs1805097
rs1805097
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs2241745
rs2241745
0.882 0.120 13 109770184 intron variant C/T snv 0.88
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2289046
rs2289046
0.827 0.240 13 109755559 3 prime UTR variant T/C snv 0.27
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs754204
rs754204
0.925 0.080 13 109759221 intron variant C/T snv 0.41
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008