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: rs159963
rs159963
3 1.000 0.040 1 8444361 intron variant C/A snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs2252865
rs2252865
6 0.851 0.040 1 8362616 intron variant T/C snv 0.72 0.700 1.000 1 2013 2013
dbSNP: rs301795
rs301795
1 1.000 0.040 1 8407293 intron variant G/A snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs301799
rs301799
1 1.000 0.040 1 8429242 intron variant C/T snv 0.61 0.700 1.000 1 2019 2019
dbSNP: rs301806
rs301806
4 0.851 0.120 1 8422018 intron variant C/T snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs301807
rs301807
4 0.925 0.080 1 8424763 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs301817
rs301817
2 0.925 0.120 1 8443319 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs3795310
rs3795310
2 1.000 0.040 1 8371547 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs6695867
rs6695867
1 1.000 0.040 1 8670720 intron variant G/A snv 0.63 0.700 1.000 1 2018 2018