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: rs2124440
rs2124440
2 2 181463487 intron variant G/A snv 0.55 0.700 1.000 3 2013 2017
dbSNP: rs1892548
rs1892548
2 13 40428504 intron variant T/A;C snv 0.700 1.000 2 2016 2018
dbSNP: rs4970966
rs4970966
2 1 150611627 intron variant G/T snv 0.16 0.700 1.000 2 2016 2018
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: rs1037171
rs1037171
2 17 74706839 intron variant G/A snv 0.53 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: 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: rs11189181
rs11189181
2 10 97384397 intron variant A/G snv 0.30 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: rs112721625
rs112721625
2 17 59850066 upstream gene variant TT/-;T;TTT;TTTT delins 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
dbSNP: rs115340020
rs115340020
2 1 92300881 intron variant G/A snv 1.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs11580646
rs11580646
2 1 117619797 intron variant C/G snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs11640143
rs11640143
2 16 85955858 regulatory region variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs11686139
rs11686139
2 2 226426699 intergenic variant A/C snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs11723763
rs11723763
2 4 144137143 intron variant G/T snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs117424492
rs117424492
2 15 79975053 upstream gene variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs117533700
rs117533700
2 19 13065914 intron variant C/G;T snv 0.700 1.000 1 2016 2016