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: rs12439144
rs12439144
1 15 78244582 intron variant G/A snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs12591810
rs12591810
1 15 78243867 intron variant A/G snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs12904669
rs12904669
1 15 78244187 intron variant C/T snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs4887023
rs4887023
2 15 78243095 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs58119220
rs58119220
1 15 78244894 intron variant C/G snv 0.37 0.700 1.000 1 2016 2016