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: rs17129789
rs17129789
2 0.925 0.080 1 67324915 intron variant T/C snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs4679904
rs4679904
2 0.925 0.080 3 160623108 intergenic variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs485499
rs485499
2 0.925 0.080 3 160028076 intron variant T/C snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs4938534
rs4938534
2 0.925 0.080 11 111404408 intron variant G/A snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs538147
rs538147
2 0.925 0.080 11 64362250 intron variant G/A snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs6890853
rs6890853
2 0.925 0.080 5 35852209 upstream gene variant G/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs7208487
rs7208487
4 0.925 0.080 17 39387196 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs7665590
rs7665590
2 0.925 0.080 4 98875633 3 prime UTR variant T/C snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs8017161
rs8017161
2 0.925 0.080 14 103096858 intron variant G/A snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs860413
rs860413
2 0.925 0.080 5 35942940 upstream gene variant A/C snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs968451
rs968451
2 0.925 0.080 22 39274846 intron variant G/T snv 0.18 0.700 1.000 1 2011 2011