rs377767406, RET

N. diseases: 9
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 0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.710 1.000 8 1995 2017
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.700 1.000 7 1995 2012
Adrenal Gland Pheochromocytoma
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
50 0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.030 1.000 3 2006 2017
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.030 1.000 3 2006 2017
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.020 1.000 2 2006 2012
Adult Anaplastic Ependymoma
CUI: C0280787
Disease: Adult Anaplastic Ependymoma
1 0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.010 1.000 1 2017 2017
Anaplastic Ependymoma
CUI: C0280788
Disease: Anaplastic Ependymoma
1 0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.010 1.000 1 2017 2017
Childhood Anaplastic Ependymoma
CUI: C4086151
Disease: Childhood Anaplastic Ependymoma
1 0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.010 1.000 1 2017 2017
Multiple Endocrine Neoplasia
CUI: C0027662
Disease: Multiple Endocrine Neoplasia
11 0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.010 1.000 1 2006 2006