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: rs2245214
rs2245214
6 0.827 0.240 6 106214866 intron variant C/G snv 0.42 0.010 1.000 1 2018 2018
dbSNP: rs6568431
rs6568431
7 0.790 0.320 6 106140931 intron variant A/C snv 0.61 0.010 1.000 1 2018 2018