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: rs3746544
rs3746544
10 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 0.040 1.000 4 2007 2018
dbSNP: rs1051312
rs1051312
5 0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 0.030 0.667 3 2007 2013
dbSNP: rs8636
rs8636
1 1.000 0.040 20 10307094 3 prime UTR variant T/A;C snv 0.020 1.000 2 2012 2017
dbSNP: rs362549
rs362549
1 1.000 0.040 20 10289242 intron variant A/G snv 0.56 0.010 1.000 1 2011 2011
dbSNP: rs362569
rs362569
1 1.000 0.040 20 10266085 intron variant T/C snv 0.38 0.010 1.000 1 2012 2012
dbSNP: rs362990
rs362990
1 1.000 0.040 20 10295573 intron variant A/T snv 0.23 0.010 1.000 1 2019 2019
dbSNP: rs362998
rs362998
1 1.000 0.040 20 10296973 synonymous variant C/T snv 0.11 0.11 0.010 1.000 1 2017 2017
dbSNP: rs6108461
rs6108461
1 1.000 0.040 20 10286622 intron variant A/G snv 0.57 0.010 1.000 1 2017 2017