rs1555166368, MEN1

N. diseases: 6
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.
Abnormality of calcium homeostasis
CUI: C4025337
Disease: Abnormality of calcium homeostasis
1 0.851 0.120 11 64809738 frameshift variant GA/- del 0.700 0
Calcium nephrolithiasis
CUI: C1855801
Disease: Calcium nephrolithiasis
1 0.851 0.120 11 64809738 frameshift variant GA/- del 0.700 0
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
39 0.851 0.120 11 64809738 frameshift variant GA/- del 0.700 0
insulinoma
CUI: C0021670
Disease: insulinoma
8 0.851 0.120 11 64809738 frameshift variant GA/- del 0.700 0
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.851 0.120 11 64809738 frameshift variant GA/- del 0.700 0
Parathyroid Adenoma
CUI: C0262587
Disease: Parathyroid Adenoma
12 0.851 0.120 11 64809738 frameshift variant GA/- del 0.700 0