rs142698837, TG

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.
Endemic goiter
CUI: C0018022
Disease: Endemic goiter
3 0.851 0.080 8 132869781 missense variant G/A snv 7.6E-04 7.0E-04 0.700 0
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.851 0.080 8 132869781 missense variant G/A snv 7.6E-04 7.0E-04 0.700 0
Intellectual Disability
CUI: C3714756
Disease: Intellectual Disability
159 0.851 0.080 8 132869781 missense variant G/A snv 7.6E-04 7.0E-04 0.700 0
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.851 0.080 8 132869781 missense variant G/A snv 7.6E-04 7.0E-04 0.700 0
Thyroid Dyshormonogenesis 3
CUI: C0342194
Disease: Thyroid Dyshormonogenesis 3
16 0.851 0.080 8 132869781 missense variant G/A snv 7.6E-04 7.0E-04 0.700 0