rs397515564, WASHC5

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 8, autosomal dominant
12 0.925 0.120 8 125055601 missense variant C/G;T snv 0.800 1.000 6 2007 2014
Hereditary Autosomal Dominant Spastic Paraplegia
7 0.925 0.120 8 125055601 missense variant C/G;T snv 0.010 1.000 1 2013 2013