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: rs10098310
rs10098310
3 8 129601368 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10147992
rs10147992
3 14 25034593 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10956483
rs10956483
3 8 129559864 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs12988934
rs12988934
3 2 181458938 non coding transcript exon variant C/T snv 5.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs7578982
rs7578982
4 2 111078961 intron variant T/C snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs2273788
rs2273788
2 9 111586337 intron variant C/T snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs2712381
rs2712381
2 3 128619757 downstream gene variant A/C snv 0.61 0.700 1.000 1 2013 2013
dbSNP: rs424971
rs424971
2 16 85912844 intron variant T/C snv 0.53 0.700 1.000 1 2013 2013
dbSNP: rs3095254
rs3095254
3 6 31253891 intergenic variant C/A;G snv 0.55 0.700 1.000 2 2011 2014
dbSNP: rs12346772
rs12346772
2 9 111158319 intron variant A/G snv 0.18 0.700 1.000 1 2014 2014
dbSNP: rs1375493
rs1375493
3 2 181459039 non coding transcript exon variant G/A snv 0.56 0.700 1.000 1 2014 2014
dbSNP: rs2047076
rs2047076
2 5 76762684 intergenic variant C/T snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs2228467
rs2228467
8 1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 0.700 1.000 2 2013 2016
dbSNP: rs10168795
rs10168795
2 2 224888625 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs1037171
rs1037171
2 17 74706839 intron variant G/A snv 0.53 0.700 1.000 1 2016 2016
dbSNP: rs10418046
rs10418046
3 19 53824615 upstream gene variant T/G snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs1042133
rs1042133
2 6 33080829 missense variant G/C snv 0.14 0.15 0.700 1.000 1 2016 2016
dbSNP: rs10489481
rs10489481
2 1 185422035 regulatory region variant G/A snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs10562650
rs10562650
2 2 181459460 intron variant TT/-;T;TTT delins 0.56 0.700 1.000 1 2016 2016
dbSNP: rs10751647
rs10751647
2 11 306884 upstream gene variant T/C snv 0.49 0.700 1.000 1 2016 2016
dbSNP: rs1105527
rs1105527
2 17 27521170 intron variant C/T snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs11086102
rs11086102
6 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2016 2016
dbSNP: rs11189181
rs11189181
2 10 97384397 intron variant A/G snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs11190141
rs11190141
3 1.000 0.040 10 99532633 upstream gene variant C/T snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs112313229
rs112313229
2 3 46323369 intergenic variant G/A;T snv 0.700 1.000 1 2016 2016