rs587776888, GJC2

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
CUI: C0037772
Disease: Spastic Paraplegia
93 0.925 0.160 1 228149860 upstream gene variant A/G snv 0.700 1.000 5 2010 2014
Leukodystrophy, Hypomyelinating, 2
CUI: C1837355
Disease: Leukodystrophy, Hypomyelinating, 2
14 0.925 0.160 1 228149860 upstream gene variant A/G snv 0.700 1.000 3 2010 2016