rs1206969193, RET

N. diseases: 2
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.
Amyloidosis, Primary Cutaneous
CUI: C0268397
Disease: Amyloidosis, Primary Cutaneous
10 0.925 0.200 10 43112117 missense variant G/A snv 0.010 1.000 1 2015 2015
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.925 0.200 10 43112117 missense variant G/A snv 0.010 1.000 1 2015 2015