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: 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: rs911263
rs911263
4 0.851 0.200 14 68286876 intron variant C/T snv 0.57 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
dbSNP: rs2293370
rs2293370
3 0.882 0.160 3 119501087 intron variant G/A snv 0.18 0.700 1.000 2 2011 2012
dbSNP: rs9303277
rs9303277
9 0.790 0.240 17 39820216 intron variant C/T snv 0.52 0.700 1.000 2 2010 2012
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: rs4979462
rs4979462
7 0.790 0.240 9 114804733 intron variant C/T snv 0.13 0.700 1.000 1 2012 2012
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: rs7574865
rs7574865
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.700 1.000 1 2012 2012
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