rs121908510, SPAST

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.
Spastic paraplegia 4, autosomal dominant
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
101 0.925 0.240 2 32136898 missense variant G/A snv 0.800 1.000 20 1999 2014
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.925 0.240 2 32136898 missense variant G/A snv 0.010 1.000 1 2019 2019