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: rs416981
rs416981
MX2
3 0.882 0.080 21 41373487 intron variant G/A snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs45575338
rs45575338
3 0.882 0.080 10 5742188 missense variant A/C;G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs4670813
rs4670813
3 0.882 0.080 2 38090568 intron variant G/A snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs4731207
rs4731207
3 0.882 0.080 7 124756591 intron variant G/A snv 0.47 0.700 1.000 1 2015 2015
dbSNP: rs4731742
rs4731742
3 0.882 0.080 7 131070053 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs4778138
rs4778138
6 0.851 0.080 15 28090674 intron variant A/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs55875066
rs55875066
3 0.882 0.080 2 239154306 intron variant C/T snv 6.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs56238684
rs56238684
4 0.882 0.080 20 34648892 intron variant G/C snv 4.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs600951
rs600951
3 0.882 0.080 9 224742 intron variant A/G snv 0.61 0.700 1.000 1 2018 2018
dbSNP: rs6750047
rs6750047
4 0.851 0.080 2 38049406 intron variant A/G snv 0.61 0.700 1.000 1 2015 2015
dbSNP: rs6914598
rs6914598
4 0.851 0.080 6 21163688 intron variant T/C snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs7041168
rs7041168
3 0.882 0.080 9 107936435 intergenic variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs72704658
rs72704658
3 0.882 0.080 1 150860534 intron variant T/C snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs73008229
rs73008229
3 0.882 0.080 11 108316962 intron variant G/A snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs75570604
rs75570604
4 0.851 0.080 16 89780269 intron variant G/C snv 4.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs75691080
rs75691080
3 0.882 0.080 20 63638397 downstream gene variant C/T snv 9.1E-02 0.700 1.000 1 2015 2015
dbSNP: rs869329
rs869329
4 0.851 0.080 9 21804694 intron variant A/G;T snv 0.700 1.000 1 2018 2018