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: rs1051336
rs1051336
2 0.925 0.120 6 32444815 3 prime UTR variant G/A;C snv 0.15 0.010 1.000 1 2018 2018
dbSNP: rs1074532
rs1074532
1 1.000 0.080 4 65791342 intergenic variant A/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs11218708
rs11218708
1 1.000 0.080 11 122601355 regulatory region variant G/A snv 0.19 0.710 1.000 1 2018 2018
dbSNP: rs12660382
rs12660382
3 0.882 0.200 6 31475546 intron variant C/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs17315309
rs17315309
1 1.000 0.080 8 52295127 intron variant A/G;T snv 0.12 0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
43 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 0.010 1.000 1 2019 2019
dbSNP: rs1800872
rs1800872
119 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2020 2020
dbSNP: rs1980495
rs1980495
2 0.925 0.160 6 32379017 intron variant A/C snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs2071286
rs2071286
12 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs2244839
rs2244839
3 0.882 0.200 6 31470591 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2246618
rs2246618
3 0.882 0.160 6 31511209 upstream gene variant C/T snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs2395157
rs2395157
5 0.827 0.240 6 32380368 intron variant A/G snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs2395163
rs2395163
3 0.882 0.160 6 32420032 intergenic variant T/C snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs2395488
rs2395488
3 0.882 0.160 6 31478132 non coding transcript exon variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs2516049
rs2516049
12 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs2516424
rs2516424
2 0.925 0.160 6 31480538 non coding transcript exon variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs2523647
rs2523647
1 1.000 0.080 6 31482001 intron variant A/G snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs28362491
rs28362491
56 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2019 2019
dbSNP: rs28483633
rs28483633
1 1.000 0.080 6 32657097 upstream gene variant C/A snv 2.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs2858331
rs2858331
5 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs361525
rs361525
TNF
62 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2019 2019
dbSNP: rs3763309
rs3763309
3 0.882 0.160 6 32408196 upstream gene variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3892710
rs3892710
4 0.851 0.240 6 32715085 upstream gene variant C/T snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs3916765
rs3916765
3 0.882 0.200 6 32717773 upstream gene variant G/A snv 8.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs4073
rs4073
64 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2019 2019