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 0.030 1.000 3 2007 2016
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 2018
dbSNP: rs13306435
rs13306435
IL6
1 1.000 0.080 7 22731420 missense variant T/A;C snv 2.9E-02; 4.2E-06 0.010 1.000 1 2011 2011