rs77503355, 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 43113655 missense variant G/A;C;T snv 0.810 1.000 19 1994 2017
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.800 1.000 8 1996 2017
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.730 1.000 3 1998 2009
Multiple endocrine neoplasia Type 2
CUI: C4048306
Disease: Multiple endocrine neoplasia Type 2
38 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.710 1.000 19 1993 2011
Multiple Endocrine Neoplasia Type 2b
CUI: C0025269
Disease: Multiple Endocrine Neoplasia Type 2b
21 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.710 1.000 10 1994 2011
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.710 1.000 2 1997 2015
Multiple Endocrine Neoplasia Type 1
CUI: C0025267
Disease: Multiple Endocrine Neoplasia Type 1
156 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.700 1.000 1 1997 1997
Multiple Endocrine Neoplasia, Type IV
CUI: C1970712
Disease: Multiple Endocrine Neoplasia, Type IV
23 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.700 1.000 1 1997 1997