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: rs4757391
rs4757391
2 11 16281393 intron variant C/T snv 0.78 0.700 1.000 2 2015 2017
dbSNP: rs1156725
rs1156725
3 11 16286154 intron variant C/T snv 0.78 0.700 1.000 1 2016 2016
dbSNP: rs12799126
rs12799126
3 11 16286917 intron variant G/T snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs1401454
rs1401454
3 11 16228637 intron variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs146669915
rs146669915
1 11 16269264 intron variant -/CTGT delins 0.700 1.000 1 2019 2019
dbSNP: rs2014408
rs2014408
3 11 16343736 intron variant C/T snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs7118275
rs7118275
2 11 16250132 intron variant C/T snv 0.78 0.700 1.000 1 2018 2018
dbSNP: rs9971406
rs9971406
1 11 16256743 intron variant G/T snv 0.78 0.700 1.000 1 2018 2018