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: rs1058587
rs1058587
4 0.882 0.200 19 18388612 missense variant C/G;T snv 0.24; 9.1E-06 0.020 1.000 2 2006 2018