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: rs3766355
rs3766355
3 0.882 0.040 1 78491756 intron variant C/A;T snv 0.020 1.000 2 2015 2016
dbSNP: rs12093097
rs12093097
1 1.000 0.040 1 78489470 intron variant C/T snv 0.25 0.010 1.000 1 2014 2014
dbSNP: rs3753380
rs3753380
1 1.000 0.040 1 78490747 intron variant T/C snv 0.78 0.010 1.000 1 2015 2015