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: rs4820408
rs4820408
1 22 40208941 intron variant T/A;G snv 0.700 1.000 3 2015 2018
dbSNP: rs139913
rs139913
1 22 40317857 intron variant T/A snv 0.69 0.700 1.000 2 2017 2018
dbSNP: rs12484438
rs12484438
1 22 40162060 intron variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs12628051
rs12628051
1 22 40258272 intron variant T/C snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs4820410
rs4820410
1 22 40294381 intron variant A/G snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs733381
rs733381
2 22 40273644 intron variant A/G snv 0.28 0.19 0.700 1.000 1 2019 2019