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: rs11123816
rs11123816
1 2 100167191 intron variant G/A snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs12712073
rs12712073
1 2 100188666 intron variant T/C snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs13001130
rs13001130
1 2 100052237 intron variant G/A snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs13023088
rs13023088
1 2 99959842 intron variant C/T snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs13032879
rs13032879
1 2 99986297 intron variant C/T snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs2043007
rs2043007
1 2 99732211 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2309752
rs2309752
1 2 100145707 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs34321437
rs34321437
1 2 99960959 intron variant C/T snv 2.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs34506349
rs34506349
1 2 99982264 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs34795510
rs34795510
1 2 99992378 intron variant C/T snv 2.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs4851250
rs4851250
1 2 100112831 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs4851254
rs4851254
1 2 100146475 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs55779933
rs55779933
1 2 99672640 intron variant C/T snv 2.5E-02 2.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs56127672
rs56127672
1 2 99988291 intron variant G/C snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs62154466
rs62154466
1 2 99575083 intron variant G/A snv 1.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs6712515
rs6712515
3 0.925 0.160 2 100190052 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs6714788
rs6714788
1 2 100069711 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6750720
rs6750720
1 2 100054283 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7579187
rs7579187
2 2 99725106 intron variant G/A snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs7583067
rs7583067
1 2 100180388 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs77179555
rs77179555
1 2 99692662 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs78633727
rs78633727
1 2 100052995 intron variant T/C snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs79785879
rs79785879
1 2 99900176 intron variant T/C snv 1.5E-02 0.700 1.000 1 2019 2019