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: rs1579050
rs1579050
3 0.925 0.040 2 152508013 intron variant A/G snv 0.42 0.700 1.000 3 2018 2018
dbSNP: rs12471183
rs12471183
1 2 152510313 intron variant T/C snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs55692468
rs55692468
1 2 152504861 intron variant T/A;G snv 0.700 1.000 1 2017 2017