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: rs6929796
rs6929796
2 1.000 0.120 6 31554892 intron variant G/A snv 0.22 0.700 1.000 2 2007 2009
dbSNP: rs2230365
rs2230365
4 0.925 0.160 6 31557671 synonymous variant C/T snv 0.16 0.13 0.700 1.000 1 2011 2011
dbSNP: rs2239705
rs2239705
1 1.000 0.120 6 31545625 intron variant G/A snv 0.18 0.16 0.700 1.000 1 2009 2009
dbSNP: rs2523503
rs2523503
1 1.000 0.120 6 31545782 non coding transcript exon variant C/A snv 0.15 0.700 1.000 1 2011 2011