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: rs10923398
rs10923398
2 1 117708553 regulatory region variant A/C snv 0.16 0.700 1.000 3 2016 2019
dbSNP: rs17534202
rs17534202
7 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 0.700 1.000 3 2016 2019
dbSNP: rs183034862
rs183034862
3 2 168457008 intron variant C/T snv 1.8E-02 0.700 1.000 3 2016 2019
dbSNP: rs2068229
rs2068229
2 3 141904462 intron variant A/G snv 0.35 0.700 1.000 3 2016 2019
dbSNP: rs3208787
rs3208787
4 17 81558634 3 prime UTR variant A/G snv 0.24 0.700 1.000 3 2016 2019
dbSNP: rs35188965
rs35188965
12 5 1104823 intron variant C/G;T snv 0.700 1.000 3 2016 2019
dbSNP: rs4332427
rs4332427
3 10 24569461 intergenic variant A/G snv 0.21 0.700 1.000 3 2016 2019
dbSNP: rs4672497
rs4672497
5 2 62296430 TF binding site variant C/G;T snv 0.700 1.000 3 2016 2019
dbSNP: rs6730558
rs6730558
5 2 8616053 intron variant C/T snv 0.47 0.700 1.000 3 2016 2019
dbSNP: rs7148979
rs7148979
2 14 74080615 intron variant T/A snv 0.17 0.700 1.000 3 2016 2019
dbSNP: rs73660574
rs73660574
3 9 132985025 intron variant G/A snv 5.3E-02 0.700 1.000 3 2016 2019
dbSNP: rs7606173
rs7606173
5 1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 0.700 1.000 3 2016 2019
dbSNP: rs8013143
rs8013143
4 14 23025068 intron variant A/G snv 0.43 0.700 1.000 3 2016 2019
dbSNP: rs8050500
rs8050500
2 16 31393250 upstream gene variant T/C snv 0.45 0.700 1.000 3 2016 2019
dbSNP: rs8067342
rs8067342
3 17 21253548 upstream gene variant C/T snv 0.25 0.700 1.000 3 2016 2019
dbSNP: rs9898189
rs9898189
2 17 82522640 intron variant C/A;G snv 0.700 1.000 3 2016 2019
dbSNP: rs10210385
rs10210385
2 2 58770577 intron variant T/C snv 0.40 0.700 1.000 2 2017 2019
dbSNP: rs10405535
rs10405535
2 19 32581179 upstream gene variant A/G;T snv 0.700 1.000 2 2016 2017
dbSNP: rs1046321
rs1046321
2 17 35575265 3 prime UTR variant T/C snv 0.38 0.700 1.000 2 2016 2017
dbSNP: rs10988207
rs10988207
2 9 129104851 intron variant G/A;C;T snv 0.700 1.000 2 2016 2017
dbSNP: rs11030967
rs11030967
2 11 4107890 intron variant C/T snv 0.51 0.700 1.000 2 2016 2019
dbSNP: rs11133613
rs11133613
2 5 1074936 intron variant A/G snv 0.91 0.700 1.000 2 2016 2017
dbSNP: rs111910553
rs111910553
2 5 1058272 intron variant G/A snv 1.1E-02 0.700 1.000 2 2016 2017
dbSNP: rs112233623
rs112233623
5 6 41957260 intron variant C/T snv 7.0E-03 0.700 1.000 2 2016 2017
dbSNP: rs11265038
rs11265038
2 1 158626052 intron variant C/A snv 0.27 0.700 1.000 2 2016 2017