rs377767404, RET

N. diseases: 11
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.
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.742 0.160 10 43114488 missense variant T/C snv 0.730 1.000 4 1999 2017
Multiple endocrine neoplasia Type 2
CUI: C4048306
Disease: Multiple endocrine neoplasia Type 2
38 0.742 0.160 10 43114488 missense variant T/C snv 0.700 1.000 8 1997 2015
Multiple Endocrine Neoplasia Type 1
CUI: C0025267
Disease: Multiple Endocrine Neoplasia Type 1
156 0.742 0.160 10 43114488 missense variant T/C snv 0.700 1.000 1 1999 1999
Multiple Endocrine Neoplasia Type 2a
CUI: C0025268
Disease: Multiple Endocrine Neoplasia Type 2a
44 0.742 0.160 10 43114488 missense variant T/C snv 0.700 1.000 1 1999 1999
Multiple Endocrine Neoplasia Type 2b
CUI: C0025269
Disease: Multiple Endocrine Neoplasia Type 2b
21 0.742 0.160 10 43114488 missense variant T/C snv 0.700 1.000 1 1999 1999
Multiple Endocrine Neoplasia, Type IV
CUI: C1970712
Disease: Multiple Endocrine Neoplasia, Type IV
23 0.742 0.160 10 43114488 missense variant T/C snv 0.700 1.000 1 1999 1999
Adrenal Gland Pheochromocytoma
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
50 0.742 0.160 10 43114488 missense variant T/C snv 0.010 1.000 1 2005 2005
C-cell hyperplasia of thyroid
CUI: C0342190
Disease: C-cell hyperplasia of thyroid
16 0.742 0.160 10 43114488 missense variant T/C snv 0.010 1.000 1 2004 2004
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.742 0.160 10 43114488 missense variant T/C snv 0.010 1.000 1 2004 2004
Hyperparathyroidism
CUI: C0020502
Disease: Hyperparathyroidism
14 0.742 0.160 10 43114488 missense variant T/C snv 0.010 1.000 1 2005 2005
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.742 0.160 10 43114488 missense variant T/C snv 0.010 1.000 1 2005 2005