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: rs1000592
rs1000592
1 1.000 0.040 2 118939624 upstream gene variant C/A snv 6.4E-03 0.010 1.000 1 2014 2014
dbSNP: rs1000952
rs1000952
1 1.000 0.040 3 184038034 missense variant G/A;C;T snv 0.66; 3.6E-05; 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs10042486
rs10042486
4 0.882 0.040 5 63965502 intron variant C/T snv 0.58 0.010 1.000 1 2019 2019
dbSNP: rs10070190
rs10070190
2 0.925 0.040 5 26866262 intergenic variant G/A snv 0.60 0.010 1.000 1 2013 2013
dbSNP: rs10491734
rs10491734
1 1.000 0.040 9 4482706 intergenic variant T/A;C snv 0.020 1.000 2 2013 2013
dbSNP: rs1059004
rs1059004
4 0.925 0.040 21 33028155 3 prime UTR variant C/A snv 0.41 0.020 1.000 2 2007 2015
dbSNP: rs11149058
rs11149058
2 0.925 0.120 13 76978136 downstream gene variant T/A;C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs11174202
rs11174202
2 0.925 0.040 12 61858476 intron variant A/G snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs1148374
rs1148374
1 1.000 0.040 18 28070318 intron variant T/A snv 0.31 0.010 1.000 1 2016 2016
dbSNP: rs11583978
rs11583978
2 0.925 0.040 1 34864921 downstream gene variant A/C;G snv 0.010 1.000 1 2011 2011
dbSNP: rs1176744
rs1176744
19 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 0.010 1.000 1 2016 2016
dbSNP: rs11783752
rs11783752
2 0.925 0.040 8 20192013 intergenic variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs11854486
rs11854486
1 1.000 0.040 15 50660473 intron variant T/C snv 7.3E-02 0.010 1.000 1 2012 2012
dbSNP: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 < 0.001 1 2020 2020
dbSNP: rs12504244
rs12504244
2 0.925 0.040 4 54619021 intergenic variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12536521
rs12536521
1 1.000 0.040 7 89349373 intergenic variant T/A snv 4.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs12605662
rs12605662
1 1.000 0.040 18 28171702 intron variant G/A snv 0.48 0.010 1.000 1 2016 2016
dbSNP: rs12635725
rs12635725
1 1.000 0.040 3 1895465 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1265692223
rs1265692223
1 1.000 0.040 3 184100530 missense variant A/G snv 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs12682807
rs12682807
1 1.000 0.040 9 4574022 splice region variant A/C snv 0.11 8.5E-02 0.010 1.000 1 2013 2013
dbSNP: rs13046814
rs13046814
1 1.000 0.040 21 33029069 3 prime UTR variant T/G snv 0.26 0.010 1.000 1 2007 2007
dbSNP: rs13316193
rs13316193
4 0.882 0.040 3 8761057 intron variant T/C snv 0.45 0.010 < 0.001 1 2017 2017
dbSNP: rs1417182
rs1417182
1 1.000 0.040 6 101885466 intron variant G/A snv 0.40 0.010 1.000 1 2011 2011
dbSNP: rs1477437491
rs1477437491
2 0.925 0.040 1 162367213 missense variant G/A snv 2.8E-05 0.010 1.000 1 2010 2010
dbSNP: rs150504822
rs150504822
1 1.000 0.040 13 83880256 missense variant T/A snv 1.3E-03 1.2E-03 0.010 1.000 1 2013 2013