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: rs2681472
rs2681472
9 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.700 1.000 2 2015 2017
dbSNP: rs2681492
rs2681492
10 0.925 0.040 12 89619312 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs57481061
rs57481061
1 1.000 0.040 12 89625401 intron variant C/G snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs12817819
rs12817819
3 0.882 0.040 12 89645549 intron variant C/T snv 9.4E-02 0.010 1.000 1 2014 2014
dbSNP: rs12818945
rs12818945
1 1.000 0.040 12 89624457 intron variant C/A snv 4.5E-02 0.010 1.000 1 2016 2016