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: rs1212171
rs1212171
8 0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 0.010 1.000 1 2017 2017
dbSNP: rs1229030855
rs1229030855
4 0.925 0.080 12 56428321 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2009 2009
dbSNP: rs28933385
rs28933385
25 0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs35275025
rs35275025
3 1.000 0.080 17 8141219 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs4719714
rs4719714
5 1.000 0.080 7 22721094 intron variant A/T snv 0.21 0.010 1.000 1 2010 2010
dbSNP: rs61816761
rs61816761
43 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs767181086
rs767181086
11 0.827 0.240 1 183220922 stop gained G/A;T snv 8.0E-06; 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs9315202
rs9315202
4 0.925 0.080 13 33067879 downstream gene variant C/T snv 0.24 0.010 1.000 1 2019 2019
dbSNP: rs9563121
rs9563121
KL
4 0.925 0.080 13 33050369 intron variant C/T snv 0.26 0.010 1.000 1 2019 2019