rs77558292, RET

N. diseases: 8
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 0.776 0.160 10 43113621 missense variant T/A;C;G snv 0.810 1.000 15 1996 2017
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.776 0.160 10 43113621 missense variant T/A;C;G snv 0.710 1.000 1 2013 2013
Multiple endocrine neoplasia Type 2
CUI: C4048306
Disease: Multiple endocrine neoplasia Type 2
38 0.776 0.160 10 43113621 missense variant T/A;C;G snv 0.700 1.000 9 1996 2011
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.776 0.160 10 43113621 missense variant T/A;C;G snv 0.700 0
Adrenal Gland Pheochromocytoma
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
50 0.776 0.160 10 43113621 missense variant T/A;C;G snv 0.030 1.000 3 2005 2012
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.776 0.160 10 43113621 missense variant T/A;C;G snv 0.030 1.000 3 2005 2012
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.776 0.160 10 43113621 missense variant T/A;C;G snv 0.020 1.000 2 2005 2009
Multiple Endocrine Neoplasia
CUI: C0027662
Disease: Multiple Endocrine Neoplasia
11 0.776 0.160 10 43113621 missense variant T/A;C;G snv 0.010 1.000 1 2005 2005