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: rs9870680
rs9870680
2 0.925 0.040 3 7487868 intron variant C/T snv 0.45 0.700 1.000 1 2011 2011
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: rs779706
rs779706
1 1.000 0.040 3 7482355 intron variant G/C snv 0.41 0.010 1.000 1 2016 2016
dbSNP: rs779867
rs779867
9 0.776 0.120 3 7442784 intron variant T/C;G snv 0.010 1.000 1 2019 2019