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: rs1434282
rs1434282
6 1 199041592 non coding transcript exon variant C/T snv 0.76 0.700 1.000 3 2016 2019
dbSNP: rs10923397
rs10923397
2 1 117708521 regulatory region variant C/T snv 0.14 0.700 1.000 2 2016 2019
dbSNP: rs12127588
rs12127588
2 1 198626376 intergenic variant G/A;C;T snv 0.700 1.000 2 2010 2017
dbSNP: rs12563213
rs12563213
2 1 154318779 upstream gene variant G/C snv 0.30 0.700 1.000 2 2016 2019
dbSNP: rs1569419
rs1569419
5 1 3080038 intron variant T/C snv 0.73 0.700 1.000 2 2016 2019
dbSNP: rs17534202
rs17534202
7 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 0.700 1.000 2 2016 2019
dbSNP: rs2492301
rs2492301
4 1 37473572 intron variant T/C snv 0.53 0.700 1.000 2 2016 2019
dbSNP: rs61823972
rs61823972
4 1 205232197 intron variant A/C;T snv 0.700 1.000 2 2016 2019
dbSNP: rs10495161
rs10495161
1 1 220963330 regulatory region variant C/T snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs1078859
rs1078859
1 1 235748725 intron variant C/A snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs10801682
rs10801682
1 1 88708570 intron variant A/T snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs1085244
rs1085244
1 1 46098008 intron variant C/A snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10910476
rs10910476
2 1 234599210 regulatory region variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11119256
rs11119256
1 1 206660258 intron variant C/G snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs11119337
rs11119337
1 1 209760788 intron variant A/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs11211480
rs11211480
4 1 47227548 non coding transcript exon variant A/G snv 0.42 0.700 1.000 1 2016 2016
dbSNP: rs115159272
rs115159272
1 1 118125195 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs116135446
rs116135446
1 1 240794633 intron variant C/T snv 2.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs1172135
rs1172135
1 1 205278032 non coding transcript exon variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11807602
rs11807602
1 1 93073392 intergenic variant C/G snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs11811522
rs11811522
2 1 158634353 intron variant G/A snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs12022684
rs12022684
1 1 43304847 splice region variant C/G snv 3.4E-02 1.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs12026918
rs12026918
1 1 65680563 intergenic variant C/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs12033311
rs12033311
1 1 117644577 upstream gene variant C/T snv 4.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs12037805
rs12037805
1 1 44031577 intron variant T/C snv 0.25 0.700 1.000 1 2019 2019