rs2076738, TG

N. diseases: 6
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.
Adenomatous goiter
CUI: C0311361
Disease: Adenomatous goiter
4 0.807 0.200 8 132906843 missense variant T/C snv 1.6E-05 7.0E-06 0.010 1.000 1 1999 1999
Dwarfism
CUI: C0013336
Disease: Dwarfism
77 0.807 0.200 8 132906843 missense variant T/C snv 1.6E-05 7.0E-06 0.010 1.000 1 2004 2004
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.807 0.200 8 132906843 missense variant T/C snv 1.6E-05 7.0E-06 0.010 1.000 1 1998 1998
Congenital goiter
CUI: C0349476
Disease: Congenital goiter
3 0.807 0.200 8 132906843 missense variant T/C snv 1.6E-05 7.0E-06 0.020 1.000 2 1998 1999
Congenital Hypothyroidism
CUI: C0010308
Disease: Congenital Hypothyroidism
48 0.807 0.200 8 132906843 missense variant T/C snv 1.6E-05 7.0E-06 0.030 1.000 3 1998 2004
Thyroid Dyshormonogenesis 3
CUI: C0342194
Disease: Thyroid Dyshormonogenesis 3
16 0.807 0.200 8 132906843 missense variant T/C snv 1.6E-05 7.0E-06 0.700 1.000 6 1999 2016