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: rs1800795
rs1800795
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.060 1.000 6 2007 2017
dbSNP: rs1800796
rs1800796
74 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.020 1.000 2 2007 2017
dbSNP: rs1800797
rs1800797
43 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 0.020 1.000 2 2007 2018
dbSNP: rs2069832
rs2069832
4 0.851 0.200 7 22727814 intron variant A/G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs2069861
rs2069861
IL6
2 0.925 0.080 7 22732035 upstream gene variant C/A;T snv 0.010 1.000 1 2011 2011