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: rs17249754
rs17249754
12 0.882 0.120 12 89666809 intron variant G/A snv 0.15 0.700 1.000 4 2011 2018
dbSNP: rs111478946
rs111478946
4 12 89665065 intron variant G/A snv 0.14 0.700 1.000 2 2018 2018
dbSNP: rs12579302
rs12579302
19 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 2 2017 2018
dbSNP: rs1401982
rs1401982
4 12 89595822 intron variant G/A snv 0.60 0.700 1.000 2 2018 2018
dbSNP: rs2681472
rs2681472
9 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.700 1.000 2 2016 2018
dbSNP: rs11105352
rs11105352
4 12 89632685 intron variant G/A snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs11105364
rs11105364
4 12 89675499 intron variant T/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs2681485
rs2681485
3 12 89631845 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2681492
rs2681492
10 0.925 0.040 12 89619312 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs4842676
rs4842676
1 12 89698005 intron variant G/C;T snv 0.700 1.000 1 2018 2018