Source: UNIPROT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1064794292
rs1064794292
2 0.882 0.200 9 21974760 missense variant C/T snv 0.710 1.000 0 2009 2009
dbSNP: rs36204594
rs36204594
1 1.000 0.040 9 21971180 missense variant G/A;T snv 0.700 0