rs2235544, DIO1

N. diseases: 14
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.800 1.000 1 2013 2013
Thyroxine measurement
CUI: C0202231
Disease: Thyroxine measurement
42 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.700 1.000 2 2013 2015
Hormone measurement
CUI: C0441683
Disease: Hormone measurement
134 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.700 1.000 1 2013 2013
Thyroid stimulating hormone measurement
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
83 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.700 1.000 1 2013 2013
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2019 2019
Adult Meningioma
CUI: C0278877
Disease: Adult Meningioma
30 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2019 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2018 2018
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2019 2019
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2019 2019
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2019 2019
Glioma
CUI: C0017638
Disease: Glioma
353 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2018 2018
Meningioma
CUI: C0025286
Disease: Meningioma
43 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2019 2019
Meningioma, benign, no ICD-O subtype
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
30 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2019 2019