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 1 2011 2011
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 2009 2009