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: rs13320980
rs13320980
1 1.000 0.040 3 119890313 intron variant T/C snv 0.23 0.010 1.000 1 2011 2011
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: rs334535
rs334535
3 0.882 0.040 3 120073457 intron variant C/T snv 0.29 0.010 1.000 1 2015 2015
dbSNP: rs4072520
rs4072520
1 1.000 0.040 3 119916546 intron variant C/A;G snv 0.010 1.000 1 2008 2008
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: rs6779828
rs6779828
2 0.925 0.120 3 120056300 intron variant C/T snv 0.28 0.010 1.000 1 2008 2008
dbSNP: rs7431209
rs7431209
1 1.000 0.040 3 119922595 intron variant A/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs3755557
rs3755557
6 0.807 0.280 3 120096110 non coding transcript exon variant T/A snv 0.14 0.030 1.000 3 2011 2020
dbSNP: rs334558
rs334558
20 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 0.020 1.000 2 2013 2017