rs150594290, ALPL

N. diseases: 3
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.
Convulsions
CUI: C4048158
Disease: Convulsions
4 1.000 0.080 1 21575894 missense variant G/A snv 0.010 1.000 1 2002 2002
Hypophosphatasia
CUI: C0020630
Disease: Hypophosphatasia
29 1.000 0.080 1 21575894 missense variant G/A snv 0.010 1.000 1 2002 2002
Seizures
CUI: C0036572
Disease: Seizures
553 1.000 0.080 1 21575894 missense variant G/A snv 0.010 1.000 1 2002 2002