rs28928896, KRT17

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.
Steatocystoma multiplex
CUI: C0259771
Disease: Steatocystoma multiplex
4 0.925 0.080 17 41624236 missense variant T/C;G snv 0.810 1.000 3 1997 2006
Pachyonychia Congenita, Type 2 (disorder)
CUI: C1721007
Disease: Pachyonychia Congenita, Type 2 (disorder)
13 0.925 0.080 17 41624236 missense variant T/C;G snv 0.800 1.000 18 1995 2013