rs965513, PTCSC2

N. diseases: 15
Disease: Familial (FPAH) ×
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.
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.742 0.200 9 97793827 intron variant A/G;T snv 0.010 1.000 1 2012 2012