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: rs10761731
rs10761731
6 10 63267850 intron variant A/T snv 0.38 0.800 1.000 4 2010 2019
dbSNP: rs10822145
rs10822145
1 10 63174788 intron variant C/T snv 0.44 0.700 1.000 2 2015 2018
dbSNP: rs2893919
rs2893919
1 10 63375018 intron variant G/A snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs3999089
rs3999089
2 10 63444048 intron variant A/G snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs7902343
rs7902343
2 10 63245639 intron variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs7916868
rs7916868
3 10 63229171 intron variant A/T snv 0.47 0.700 1.000 1 2018 2018