rs377767405, RET

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.
Multiple Endocrine Neoplasia Type 2a
CUI: C0025268
Disease: Multiple Endocrine Neoplasia Type 2a
44 0.827 0.120 10 43114489 missense variant G/A;C;T snv 0.710 1.000 1 2007 2007
Multiple endocrine neoplasia Type 2
CUI: C4048306
Disease: Multiple endocrine neoplasia Type 2
38 0.827 0.120 10 43114489 missense variant G/A;C;T snv 0.700 1.000 11 1995 2015
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.827 0.120 10 43114489 missense variant G/A;C;T snv 0.700 0
Adrenal Gland Pheochromocytoma
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
50 0.827 0.120 10 43114489 missense variant G/A;C;T snv 0.010 1.000 1 1998 1998
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.827 0.120 10 43114489 missense variant G/A;C;T snv 0.010 1.000 1 1998 1998