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: rs7082066
rs7082066
2 10 63239211 intron variant A/G snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs7085862
rs7085862
1 10 63486687 intron variant T/G snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs7899503
rs7899503
2 10 63327708 intron variant C/G;T snv 0.700 1.000 1 2018 2018