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: rs6790167
rs6790167
5 0.827 0.080 3 189869485 intron variant A/G snv 0.53 0.010 1.000 1 2016 2016
dbSNP: rs11571833
rs11571833
31 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 0.710 1.000 1 2017 2018
dbSNP: rs3124599
rs3124599
5 0.851 0.080 9 136509318 intron variant G/A snv 0.13 0.010 1.000 1 2017 2017
dbSNP: rs312599
rs312599
1 1.000 0.080 5 143998425 intergenic variant C/T snv 0.33 0.010 1.000 1 2017 2017
dbSNP: rs942190
rs942190
2 1.000 0.080 14 89956320 intron variant T/C snv 0.37 0.010 1.000 1 2017 2017
dbSNP: rs1412125
rs1412125
17 0.724 0.360 13 30467458 intron variant C/G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs4759314
rs4759314
31 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 0.010 1.000 1 2018 2018
dbSNP: rs859
rs859
6 0.807 0.200 15 81308981 3 prime UTR variant A/G snv 0.33 0.010 1.000 1 2018 2018
dbSNP: rs13181
rs13181
134 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 0.010 1.000 1 2019 2019
dbSNP: rs4513061
rs4513061
6 0.807 0.080 15 86428401 intron variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs12666409
rs12666409
DDC
1 1.000 0.080 7 50567279 upstream gene variant T/A snv 0.21 0.010 1.000 1 2020 2020