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: rs1800630
rs1800630
17 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 0.720 0.667 3 2011 2019
dbSNP: rs3093662
rs3093662
TNF
9 0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 0.700 1.000 1 2007 2007
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.070 0.857 7 2011 2019
dbSNP: rs361525
rs361525
TNF
62 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.030 1.000 3 2018 2019
dbSNP: rs1799724
rs1799724
LTA ; TNF
47 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
47 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2018 2018
dbSNP: rs1800750
rs1800750
TNF
5 0.827 0.280 6 31575186 upstream gene variant G/A snv 1.6E-02 0.010 1.000 1 2018 2018
dbSNP: rs745738344
rs745738344
TNF
28 0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 0.010 1.000 1 2018 2018