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: rs1033182
rs1033182
3 0.882 0.160 6 151873899 intron variant G/A snv 0.26 0.010 1.000 1 2007 2007
dbSNP: rs1709183
rs1709183
3 0.882 0.160 6 151872861 intron variant C/T snv 0.67 0.010 1.000 1 2007 2007
dbSNP: rs1884051
rs1884051
4 0.882 0.080 6 151962144 intron variant G/A snv 0.60 0.010 1.000 1 2008 2008
dbSNP: rs2207396
rs2207396
2 0.925 0.120 6 152061247 intron variant G/A snv 0.23 0.010 1.000 1 2013 2013
dbSNP: rs2431260
rs2431260
3 0.882 0.160 6 151871196 intron variant G/C;T snv 0.010 1.000 1 2007 2007
dbSNP: rs3020314
rs3020314
7 0.790 0.280 6 151949537 intron variant C/G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs3020317
rs3020317
1 1.000 0.080 6 151957606 intron variant C/T snv 0.77 0.010 1.000 1 2008 2008
dbSNP: rs9397456
rs9397456
3 0.882 0.160 6 151926017 intron variant A/G;T snv 0.010 1.000 1 2008 2008