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 0.040 1.000 4 2017 2018
dbSNP: rs2069837
rs2069837
18 0.724 0.520 7 22728408 intron variant A/C;G snv 0.020 1.000 2 2013 2016
dbSNP: rs1474348
rs1474348
4 0.882 0.080 7 22728289 intron variant C/G snv 0.71 0.010 1.000 1 2017 2017
dbSNP: rs1800797
rs1800797
43 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 0.010 1.000 1 2009 2009
dbSNP: rs2069840
rs2069840
13 0.742 0.360 7 22728953 intron variant C/G snv 0.27 0.010 1.000 1 2017 2017
dbSNP: rs2069845
rs2069845
IL6
8 0.807 0.120 7 22730530 intron variant G/A snv 0.61 0.010 1.000 1 2017 2017