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: rs1038822
rs1038822
1 1.000 0.120 2 43511034 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs10505648
rs10505648
1 1.000 0.120 8 136144207 intron variant A/G snv 0.43 0.700 1.000 1 2015 2015
dbSNP: rs10514258
rs10514258
1 1.000 0.120 5 83575938 intron variant A/G snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs10739076
rs10739076
1 1.000 0.120 9 5440589 upstream gene variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10760321
rs10760321
1 1.000 0.120 9 124101917 TF binding site variant A/G snv 0.30 0.700 1.000 1 2015 2015
dbSNP: rs10865238
rs10865238
1 1.000 0.120 2 49041665 intron variant A/G snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs10993397
rs10993397
1 1.000 0.120 9 94917489 intron variant C/T snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs11031005
rs11031005
5 1.000 0.120 11 30204809 intron variant T/C snv 0.10 0.700 1.000 1 2018 2018
dbSNP: rs112137861
rs112137861
2 1.000 0.120 12 23857104 intron variant C/A snv 3.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs1159315
rs1159315
1 1.000 0.120 4 47001059 intron variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs11891936
rs11891936
1 1.000 0.120 2 43305163 intron variant C/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs1275468
rs1275468
1 1.000 0.120 12 75541377 intergenic variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs1355471
rs1355471
1 1.000 0.120 12 28568792 intron variant G/A snv 0.52 0.700 1.000 1 2015 2015
dbSNP: rs140485756
rs140485756
2 1.000 0.120 6 69410439 intergenic variant T/C snv 3.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs1627536
rs1627536
1 1.000 0.120 9 123780425 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17030684
rs17030684
1 1.000 0.120 2 43320989 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs1778890
rs1778890
1 1.000 0.120 9 123769476 intron variant T/C snv 0.25 0.35 0.700 1.000 1 2011 2011
dbSNP: rs1795379
rs1795379
1 1.000 0.120 12 75547262 intergenic variant T/C snv 0.70 0.700 1.000 1 2018 2018
dbSNP: rs1873555
rs1873555
1 1.000 0.120 2 43552526 intron variant T/C snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs2060941
rs2060941
1 1.000 0.120 17 39826630 intron variant G/T snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs2069408
rs2069408
2 0.925 0.200 12 55970537 intron variant A/G snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs2178575
rs2178575
1 1.000 0.120 2 212527042 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2271194
rs2271194
1 1.000 0.120 12 56083910 splice region variant A/T snv 0.63 0.53 0.700 1.000 1 2018 2018
dbSNP: rs2292239
rs2292239
13 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.700 1.000 1 2012 2012
dbSNP: rs4340576
rs4340576
1 1.000 0.120 2 43328367 intron variant T/C snv 0.80 0.700 1.000 1 2011 2011