rs11675342, TPO

N. diseases: 5
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.
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.851 0.040 2 1403856 intron variant C/T snv 0.40 0.700 1.000 3 2016 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.851 0.040 2 1403856 intron variant C/T snv 0.40 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.851 0.040 2 1403856 intron variant C/T snv 0.40 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.851 0.040 2 1403856 intron variant C/T snv 0.40 0.700 1.000 1 2019 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.851 0.040 2 1403856 intron variant C/T snv 0.40 0.700 1.000 1 2019 2019