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: rs20575
rs20575
29 0.645 0.440 8 23201811 missense variant C/G snv 0.54 0.44 0.010 1.000 1 2015 2015
dbSNP: rs2230229
rs2230229
8 0.807 0.120 8 23191779 missense variant C/T snv 0.88 0.86 0.010 1.000 1 2015 2015