rs767671406, MPRIP;FLCN

N. diseases: 2
Source: CLINVAR ×
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
6385 1.000 0.080 17 17216506 splice region variant GGA/- delins 0.700 1.000 7 2000 2017
Multiple fibrofolliculomas
CUI: C0346010
Disease: Multiple fibrofolliculomas
88 1.000 0.080 17 17216506 splice region variant GGA/- delins 0.700 1.000 6 2010 2017