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: rs6455128
rs6455128
2 1.000 0.080 6 61987841 intron variant A/C snv 0.79 0.700 1.000 1 2008 2008
dbSNP: rs2477664
rs2477664
1 10 17833817 synonymous variant T/A snv 4.5E-04 0.49 0.700 1.000 1 2010 2010
dbSNP: rs2896019
rs2896019
10 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.700 1.000 1 2010 2010
dbSNP: rs17109512
rs17109512
2 1.000 0.040 10 98367794 regulatory region variant G/A snv 9.5E-02 0.800 1.000 1 2011 2011
dbSNP: rs10198552
rs10198552
2 2 134842306 intron variant T/C snv 6.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs13077101
rs13077101
4 3 120706484 intron variant T/C snv 0.700 1.000 1 2012 2012
dbSNP: rs16840760
rs16840760
4 2 204118831 intergenic variant T/C snv 3.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs2078087
rs2078087
4 1 183389270 intron variant C/T snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs6855088
rs6855088
2 4 181783398 intergenic variant A/G snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs7825271
rs7825271
2 8 68651460 intron variant G/T snv 0.84 0.700 1.000 1 2012 2012
dbSNP: rs892295
rs892295
4 3 355870 intron variant A/G snv 0.87 0.700 1.000 1 2012 2012
dbSNP: rs4949718
rs4949718
3 1 76433779 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs596406
rs596406
1 10 11182702 intron variant T/C snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs862946
rs862946
1 14 26019261 intron variant T/C snv 0.77 0.700 1.000 1 2013 2013
dbSNP: rs11292716
rs11292716
1 7 95305887 intron variant A/- delins 0.700 1.000 1 2017 2017
dbSNP: rs757158
rs757158
5 0.851 0.240 7 95326216 upstream gene variant C/T snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs10001545
rs10001545
3 4 87254878 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10165093
rs10165093
1 2 232639279 intron variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs10509735
rs10509735
1 10 99372525 intron variant A/C snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs10827785
rs10827785
1 10 17933413 intergenic variant T/C snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs11067592
rs11067592
2 12 109631385 intergenic variant G/T snv 1.2E-03 0.700 1.000 1 2018 2018
dbSNP: rs114059064
rs114059064
1 6 33108491 upstream gene variant T/C snv 0.700 1.000 1 2018 2018
dbSNP: rs115695709
rs115695709
1 6 32223562 intron variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs11878604
rs11878604
5 19 40827379 intron variant T/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs139761834
rs139761834
3 7 80545045 intron variant T/C snv 2.8E-04 0.700 1.000 1 2018 2018