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: rs487766
rs487766
4 15 58401661 intron variant C/T snv 0.73 0.700 1.000 1 2009 2009
dbSNP: rs8033940
rs8033940
5 15 58432643 intron variant G/A snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs8034802
rs8034802
5 15 58432593 intron variant T/A snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs1800588
rs1800588
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 6 2012 2019