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: rs3771829
rs3771829
9 0.790 0.120 2 75137019 intron variant C/G snv 0.11 0.010 1.000 1 2014 2014
dbSNP: rs3771856
rs3771856
3 0.882 0.080 2 75186888 non coding transcript exon variant G/A snv 0.57 0.010 1.000 1 2010 2010
dbSNP: rs6715729
rs6715729
1 1.000 0.080 2 75198602 synonymous variant A/G snv 0.48 0.58 0.010 1.000 1 2009 2009
dbSNP: rs735668
rs735668
1 1.000 0.080 2 75135918 intron variant A/C;G snv 0.010 1.000 1 2009 2009