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: rs1828911
rs1828911
1 8 75550312 intron variant T/C;G snv 0.700 1.000 3 2018 2019
dbSNP: rs6026578
rs6026578
4 20 58888417 5 prime UTR variant C/G snv 0.60 0.700 1.000 3 2018 2019
dbSNP: rs7679724
rs7679724
1 4 9983752 intron variant G/T snv 0.65 0.700 1.000 3 2018 2019
dbSNP: rs79105258
rs79105258
24 12 111280427 intron variant C/A;T snv 0.700 1.000 3 2018 2019
dbSNP: rs11202346
rs11202346
1 10 87149155 intron variant G/T snv 0.69 0.700 1.000 2 2018 2019
dbSNP: rs143825439
rs143825439
1 11 63552521 downstream gene variant G/A;T snv 0.700 1.000 2 2018 2019
dbSNP: rs1549287
rs1549287
1 16 69556463 intergenic variant A/G snv 0.89 0.700 1.000 2 2018 2019
dbSNP: rs16856823
rs16856823
3 2 169343942 intron variant A/T snv 4.6E-02 0.700 1.000 2 2018 2019
dbSNP: rs1797052
rs1797052
2 1 145707383 5 prime UTR variant A/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs1886603
rs1886603
1 10 117722792 intergenic variant G/A snv 0.13 0.700 1.000 2 2018 2019
dbSNP: rs2075251
rs2075251
1 2 169154948 intron variant T/A;C snv 0.700 1.000 2 2018 2019
dbSNP: rs2220970
rs2220970
1 11 9836202 intron variant G/A snv 0.80 0.700 1.000 2 2018 2019
dbSNP: rs2390793
rs2390793
1 2 169348613 intron variant C/A;T snv 0.700 1.000 2 2019 2019
dbSNP: rs4724828
rs4724828
1 7 1258812 intergenic variant C/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs57633992
rs57633992
1 11 64657495 intron variant C/A;T snv 0.700 1.000 2 2018 2019
dbSNP: rs6031598
rs6031598
1 20 44427509 intron variant G/A;T snv 0.700 1.000 2 2019 2019
dbSNP: rs6445559
rs6445559
1 3 53065450 intron variant A/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs73436803
rs73436803
1 15 75326860 upstream gene variant C/G;T snv 0.700 1.000 2 2019 2019
dbSNP: rs74896528
rs74896528
1 1 28271776 missense variant C/T snv 2.2E-03 8.6E-04 0.700 1.000 2 2019 2019
dbSNP: rs7835379
rs7835379
1 8 94962852 intron variant G/A;C snv 0.700 1.000 2 2018 2019
dbSNP: rs9394948
rs9394948
1 6 43367017 intron variant A/C;G snv 0.700 1.000 2 2018 2019
dbSNP: rs9416703
rs9416703
1 10 58523248 intron variant A/C snv 0.46 0.700 1.000 2 2018 2019
dbSNP: rs9795139
rs9795139
1 11 65933988 intergenic variant T/A;C;G snv 0.700 1.000 2 2018 2019
dbSNP: rs1000791
rs1000791
1 17 79269796 intron variant T/A snv 8.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs1006207
rs1006207
1 11 64082340 intron variant C/G;T snv 0.700 1.000 1 2019 2019