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: rs3792452
rs3792452
2 0.925 0.040 3 7625097 intron variant C/T snv 0.15 0.010 1.000 1 2013 2013
dbSNP: rs6782011
rs6782011
7 0.807 0.120 3 7457960 intron variant C/T snv 0.52 0.010 1.000 1 2019 2019
dbSNP: rs779867
rs779867
9 0.776 0.120 3 7442784 intron variant T/C;G snv 0.010 1.000 1 2019 2019