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: rs11105352
rs11105352
4 12 89632685 intron variant G/A snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs111478946
rs111478946
4 12 89665065 intron variant G/A snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs12230074
rs12230074
2 12 89697090 intron variant A/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs12579302
rs12579302
19 0.851 0.120 12 89656726 intron variant A/G snv 0.15 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