rs1554867698, OAT

N. diseases: 1
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.
Gyrate Atrophy
CUI: C0018425
Disease: Gyrate Atrophy
35 1.000 0.080 10 124411967 splice donor variant ACGTACCT/TTAA delins 0.700 0