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: rs12636078
rs12636078
3 3 20064181 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2948097
rs2948097
1 3 20063934 intron variant A/G snv 0.65 0.700 1.000 1 2018 2018