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: rs603424
rs603424
13 1.000 0.080 10 100315722 intron variant G/A snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs139141690
rs139141690
3 7 101856650 intron variant G/A snv 2.2E-03 0.700 1.000 1 2016 2016
dbSNP: rs34061204
rs34061204
1 4 101878992 intron variant A/-;AA;AAA delins 0.700 1.000 1 2016 2016
dbSNP: rs412332
rs412332
1 7 102064238 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11121529
rs11121529
1 1 10211630 5 prime UTR variant C/G snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs17396340
rs17396340
3 1 10226118 intron variant G/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs11627756
rs11627756
1 14 102630269 intron variant C/T snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs944002
rs944002
3 14 103106478 intron variant A/G snv 0.25 0.800 1.000 1 2011 2011
dbSNP: rs4807455
rs4807455
1 19 1033560 intron variant G/A snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs4699154
rs4699154
2 4 105112927 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs3000073
rs3000073
1 14 105263455 intron variant G/A snv 0.28 0.800 1.000 1 2011 2011
dbSNP: rs4555082
rs4555082
2 14 105292627 intron variant C/T snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs6993770
rs6993770
9 0.925 0.080 8 105569300 intron variant A/T snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs342240
rs342240
1 7 106696804 intron variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs10274553
rs10274553
1 7 106716200 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs342293
rs342293
7 0.882 0.040 7 106731773 intron variant C/G snv 0.42 0.800 1.000 7 2009 2019
dbSNP: rs342294
rs342294
1 7 106732176 intron variant T/C snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs342295
rs342295
2 7 106732314 intron variant C/T snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs342296
rs342296
1 7 106732457 intron variant G/A snv 0.41 0.800 1.000 1 2012 2012
dbSNP: rs342298
rs342298
1 7 106733200 intron variant C/T snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs12534473
rs12534473
1 7 106734102 intron variant T/G snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs719152
rs719152
1 11 10686942 intron variant C/G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs12974537
rs12974537
1 19 1074316 intron variant C/T snv 5.7E-02 6.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs11123694
rs11123694
1 2 108448107 upstream gene variant C/T snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs987044
rs987044
1 12 108856580 intron variant A/C;G snv 0.700 1.000 1 2016 2016