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: rs11292716
rs11292716
1 7 95305887 intron variant A/- delins 0.700 1.000 1 2017 2017
dbSNP: rs10509735
rs10509735
1 10 99372525 intron variant A/C snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs1818782
rs1818782
C9 ; DAB2
3 5 39424526 intron variant A/C snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs6455128
rs6455128
2 1.000 0.080 6 61987841 intron variant A/C snv 0.79 0.700 1.000 1 2008 2008
dbSNP: rs6899983
rs6899983
1 6 31791154 intron variant A/C snv 3.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs12803802
rs12803802
1 11 107800953 intron variant A/G snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs139271658
rs139271658
2 1.000 0.040 9 9797383 intron variant A/G snv 1.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs6855088
rs6855088
2 4 181783398 intergenic variant A/G snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs686288
rs686288
1 12 100982873 intron variant A/G snv 4.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs73154660
rs73154660
1 3 157229738 intron variant A/G snv 1.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs892295
rs892295
4 3 355870 intron variant A/G snv 0.87 0.700 1.000 1 2012 2012
dbSNP: rs9389268
rs9389268
6 1.000 0.080 6 135098493 intron variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs4598207
rs4598207
2 7 50218883 intron variant A/T snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs4835265
rs4835265
6 4 145900258 intron variant C/A snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs73550818
rs73550818
1 16 58730951 intron variant C/A snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs75759936
rs75759936
3 4 78698045 intergenic variant C/A snv 5.0E-03 0.700 1.000 1 2018 2018
dbSNP: rs10001545
rs10001545
3 4 87254878 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs147627531
rs147627531
1 4 20989760 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2241339
rs2241339
3 2 169013785 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
24 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs79303598
rs79303598
1 5 65249673 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115695709
rs115695709
1 6 32223562 intron variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs117983281
rs117983281
1 9 2809077 intron variant C/T snv 1.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs11820744
rs11820744
2 1.000 0.040 11 3147308 intron variant C/T snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs12231737
rs12231737
5 0.925 0.120 12 112136812 intron variant C/T snv 5.9E-03 0.700 1.000 1 2019 2019