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: rs10733682
rs10733682
1 9 126698635 3 prime UTR variant A/G;T snv 0.700 1.000 4 2015 2019
dbSNP: rs2235056
rs2235056
1 9 126614956 intron variant C/T snv 9.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs3814120
rs3814120
1 9 126652650 intron variant G/A snv 8.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs3829849
rs3829849
2 9 126628521 intron variant C/T snv 0.28 0.700 1.000 1 2016 2016