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: rs10488631
rs10488631
7 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 0.830 1.000 3 2008 2016
dbSNP: rs12531711
rs12531711
2 0.827 0.200 7 128977412 intron variant A/C;G snv 0.800 1.000 2 2011 2017
dbSNP: rs10239340
rs10239340
1 1.000 0.080 7 129028456 intron variant T/A;G snv 0.700 1.000 3 2008 2014
dbSNP: rs10279821
rs10279821
1 1.000 0.080 7 129043493 intron variant T/A;C snv 0.700 1.000 1 2008 2008
dbSNP: rs7789423
rs7789423
1 1.000 0.080 7 128981150 intron variant A/G snv 0.64 0.700 1.000 1 2014 2014