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: rs10168795
rs10168795
2 2 224888625 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs1021479
rs1021479
2 16 85923808 upstream gene variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10276619
rs10276619
3 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 0.700 1.000 1 2018 2018
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: rs10956483
rs10956483
3 8 129559864 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs10987830
rs10987830
2 9 128016459 intergenic variant G/A snv 6.8E-03 0.700 1.000 1 2018 2018
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
dbSNP: rs112505971
rs112505971
13 10 27068541 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs112721625
rs112721625
2 17 59850066 upstream gene variant TT/-;T;TTT;TTTT delins 0.700 1.000 1 2016 2016
dbSNP: rs11327184
rs11327184
4 8 129592027 intron variant C/- delins 0.40 0.700 1.000 1 2016 2016
dbSNP: rs113760175
rs113760175
3 6 22343363 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs113899791
rs113899791
2 16 85902784 5 prime UTR variant GGCTGCAGGT/-;GGCTGCAGGTGGCTGCAGGT;GGCTGCAGGTGGCTGCAGGTGGCTGCAGGT delins 0.700 1.000 1 2016 2016
dbSNP: rs114208039
rs114208039
2 6 31273862 intron variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs115007843
rs115007843
2 4 82654059 intron variant A/C snv 0.18 0.700 1.000 1 2018 2018