rs377767395, RET

N. diseases: 4
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.
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.882 0.120 10 43113613 missense variant A/G snv 0.010 1.000 1 2016 2016
Goiter
CUI: C0018021
Disease: Goiter
19 0.882 0.120 10 43113613 missense variant A/G snv 0.010 1.000 1 2005 2005
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.882 0.120 10 43113613 missense variant A/G snv 0.010 1.000 1 2008 2008
Multiple Endocrine Neoplasia Type 2a
CUI: C0025268
Disease: Multiple Endocrine Neoplasia Type 2a
44 0.882 0.120 10 43113613 missense variant A/G snv 0.010 1.000 1 2005 2005