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: rs10494270
rs10494270
1 1 151934697 regulatory region variant A/G snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs10953730
rs10953730
2 7 113271355 intergenic variant A/C;G snv 0.25 0.700 1.000 1 2008 2008
dbSNP: rs1171606
rs1171606
3 0.925 0.120 10 59674761 intron variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs1171614
rs1171614
7 0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 0.700 1.000 1 2015 2015
dbSNP: rs1171616
rs1171616
6 0.882 0.200 10 59708831 intron variant G/T snv 0.79 0.700 1.000 1 2015 2015
dbSNP: rs12210538
rs12210538
3 1.000 0.040 6 110438805 missense variant A/G snv 0.17 0.16 0.700 1.000 1 2015 2015
dbSNP: rs2286963
rs2286963
2 2 210195326 missense variant T/G snv 0.30 0.27 0.700 1.000 1 2015 2015
dbSNP: rs270601
rs270601
1 5 132321304 intron variant T/C snv 0.71 0.700 1.000 1 2015 2015
dbSNP: rs270602
rs270602
1 5 132321007 intron variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs6893782
rs6893782
1 5 132403741 intergenic variant C/A snv 0.72 0.700 1.000 1 2015 2015
dbSNP: rs7552404
rs7552404
1 1 75670261 intron variant A/G snv 0.25 0.700 1.000 1 2015 2015
dbSNP: rs8396
rs8396
4 4 158709665 3 prime UTR variant T/C snv 0.29 0.700 1.000 1 2015 2015