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: rs1537373
rs1537373
2 0.925 0.120 9 22103342 intron variant T/G snv 0.63 0.010 1.000 1 2019 2019
dbSNP: rs3217992
rs3217992
16 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 0.010 1.000 1 2016 2016
dbSNP: rs6475609
rs6475609
2 0.925 0.120 9 22106272 intron variant A/C;G;T snv 0.010 1.000 1 2019 2019