rs77709286, RET

N. diseases: 12
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
44 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.800 1.000 27 1993 2017
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.800 0
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.730 1.000 6 2002 2017
Familial medullary thyroid carcinoma
45 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.710 1.000 21 1993 2004
Multiple endocrine neoplasia Type 2
CUI: C4048306
Disease: Multiple endocrine neoplasia Type 2
38 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.710 1.000 10 1994 2016
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.700 1.000 4 2010 2012
Multiple Endocrine Neoplasia Type 1
CUI: C0025267
Disease: Multiple Endocrine Neoplasia Type 1
156 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.700 1.000 1 1995 1995
Multiple Endocrine Neoplasia Type 2b
21 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.700 1.000 1 1995 1995
Multiple Endocrine Neoplasia, Type IV
23 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.700 1.000 1 1995 1995
C-cell hyperplasia of thyroid
CUI: C0342190
Disease: C-cell hyperplasia of thyroid
16 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.010 1.000 1 2002 2002
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.010 1.000 1 2003 2003
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.010 1.000 1 2003 2003