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: rs6830062
rs6830062
2 4 18016107 intron variant T/C snv 0.25 0.700 1.000 3 2008 2019
dbSNP: rs13131350
rs13131350
1 4 17875864 synonymous variant A/G snv 0.13 0.700 1.000 2 2015 2019
dbSNP: rs16896068
rs16896068
2 4 17943217 intron variant G/A snv 0.25 0.700 1.000 2 2008 2019
dbSNP: rs2724475
rs2724475
2 4 17944809 intron variant T/C snv 0.71 0.700 1.000 2 2010 2019
dbSNP: rs724577
rs724577
3 4 17991787 intron variant A/C snv 0.71 0.700 1.000 2 2011 2019
dbSNP: rs7692995
rs7692995
2 4 17935011 intron variant T/C snv 0.23 0.700 1.000 2 2014 2019
dbSNP: rs925098
rs925098
3 4 17918188 intron variant G/A snv 0.70 0.700 1.000 2 2012 2019
dbSNP: rs2061456
rs2061456
1 4 17996803 intron variant C/A snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs2707450
rs2707450
3 4 17940937 intron variant C/T snv 0.73 0.700 1.000 1 2019 2019
dbSNP: rs34710064
rs34710064
1 4 17963642 intron variant TT/-;T;TTT delins 0.700 1.000 1 2017 2017
dbSNP: rs35362908
rs35362908
1 4 17992675 intron variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs57654001
rs57654001
1 4 17865243 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6824748
rs6824748
2 4 17995443 intron variant G/A snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs6845078
rs6845078
2 4 17950585 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs75198716
rs75198716
1 4 17878768 intron variant T/A snv 2.3E-04 0.700 1.000 1 2019 2019
dbSNP: rs7700107
rs7700107
1 4 17878793 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs79640067
rs79640067
1 4 17878849 intron variant T/A snv 1.7E-03 0.700 1.000 1 2019 2019