rs786203385, MAX

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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 1.000 14 65077912 splice donor variant C/T snv 0.700 1.000 1 2011 2011
PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO
CUI: C3149711
Disease: PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO
9 1.000 14 65077912 splice donor variant C/T snv 0.700 0