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: rs555456
rs555456
2 0.925 0.120 11 64650787 intron variant T/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs1212146
rs1212146
2 0.925 0.120 11 64645405 intron variant A/G snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs2269730
rs2269730
2 0.925 0.120 11 64656359 intron variant G/A snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs2285339
rs2285339
2 0.925 0.120 11 64650833 intron variant G/A snv 0.26 0.700 1.000 1 2013 2013
dbSNP: rs2959654
rs2959654
2 0.925 0.120 11 64644614 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs530775
rs530775
2 0.925 0.120 11 64659461 non coding transcript exon variant A/G snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs7117423
rs7117423
3 0.925 0.120 11 64657648 intron variant G/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7128467
rs7128467
2 0.925 0.120 11 64647639 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs3825074
rs3825074
2 0.925 0.120 11 64648295 synonymous variant G/A snv 0.14 0.11 0.700 1.000 1 2013 2013