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: rs334558
rs334558
20 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 0.020 1.000 2 2008 2017
dbSNP: rs6782799
rs6782799
1 1.000 0.040 3 119891946 intron variant C/T snv 0.54 0.020 1.000 2 2010 2010
dbSNP: rs13321783
rs13321783
1 1.000 0.040 3 119896528 intron variant T/C snv 0.56 0.010 1.000 1 2008 2008
dbSNP: rs2199503
rs2199503
4 0.851 0.080 3 120059642 intron variant T/C snv 0.79 0.010 1.000 1 2015 2015
dbSNP: rs2319398
rs2319398
1 1.000 0.040 3 119894095 intron variant C/A snv 0.54 0.010 1.000 1 2008 2008
dbSNP: rs334535
rs334535
3 0.882 0.040 3 120073457 intron variant C/T snv 0.29 0.010 1.000 1 2015 2015
dbSNP: rs334555
rs334555
1 1.000 0.040 3 120085289 intron variant G/A;C;T snv 0.010 1.000 1 2010 2010
dbSNP: rs6438552
rs6438552
9 0.790 0.280 3 119912967 intron variant A/G snv 0.54 0.010 1.000 1 2014 2014
dbSNP: rs6771023
rs6771023
3 0.882 0.040 3 119974764 intron variant T/C snv 0.22 0.010 1.000 1 2015 2015
dbSNP: rs6808874
rs6808874
1 1.000 0.040 3 119839004 intron variant A/T snv 0.24 0.010 1.000 1 2008 2008