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: rs6993770
rs6993770
9 0.925 0.080 8 105569300 intron variant A/T snv 0.31 0.800 1.000 2 2011 2016
dbSNP: rs1349319
rs1349319
1 8 105544406 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs16873291
rs16873291
1 8 105515802 intron variant C/T snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs16873365
rs16873365
1 8 105546007 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs16873402
rs16873402
1 8 105577019 intron variant C/T snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs6993696
rs6993696
1 8 105569056 intron variant G/A snv 0.45 0.700 1.000 1 2011 2011
dbSNP: rs7013321
rs7013321
1 8 105581330 intron variant G/A snv 0.51 0.700 1.000 1 2011 2011