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: rs7859727
rs7859727
3 1.000 0.080 9 22102166 intron variant C/T snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs10757278
rs10757278
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.080 0.875 8 2010 2020
dbSNP: rs2383207
rs2383207
22 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.040 0.750 4 2013 2020
dbSNP: rs10757274
rs10757274
22 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.030 1.000 3 2009 2019
dbSNP: rs2383206
rs2383206
17 0.742 0.320 9 22115027 intron variant A/G snv 0.49 0.030 1.000 3 2009 2019
dbSNP: rs1333040
rs1333040
15 0.732 0.280 9 22083405 intron variant C/G;T snv 0.020 1.000 2 2013 2016
dbSNP: rs1333042
rs1333042
7 0.827 0.120 9 22103814 intron variant A/G snv 0.63 0.020 1.000 2 2013 2016
dbSNP: rs1537378
rs1537378
4 0.882 0.160 9 22061615 intron variant A/G snv 0.73 0.020 1.000 2 2010 2015
dbSNP: rs4977574
rs4977574
26 0.695 0.520 9 22098575 intron variant A/G;T snv 0.020 1.000 2 2013 2016
dbSNP: rs1333047
rs1333047
9 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2015 2015
dbSNP: rs1333049
rs1333049
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2018 2018