Source: ALL
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: rs12724990
rs12724990 		1 1 100671474 intergenic variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs221792
rs221792
GIGYF1
1 7 100681034 3 prime UTR variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1754541
rs1754541
LOC101928334
2 1 101160327 intergenic variant A/G snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs7575217
rs7575217
TBC1D8
3 2 101160470 intron variant A/G snv 0.68 0.700 1.000 1 2016 2016
dbSNP: rs7168592
rs7168592
CHSY1
4 15 101183294 intron variant C/T snv 9.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs111759324
rs111759324 		2 1 101186966 upstream gene variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs74431709
rs74431709 		1 1 101187569 upstream gene variant T/G snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs12613485
rs12613485 		1 2 101538302 intron variant G/A snv 8.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs13062095
rs13062095 		2 3 101548541 intergenic variant T/C snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs73177866
rs73177866 		1 7 101728790 regulatory region variant A/T snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs115567723
rs115567723
MAP4K4
1 2 101746707 intron variant C/T snv 1.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs111955202
rs111955202
MAP4K4
1 2 101788512 intron variant A/G snv 1.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs114743735
rs114743735
IRAK2
2 3 10186296 intron variant C/G snv 4.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs115820364
rs115820364
IRAK2
1 3 10187476 intron variant C/T snv 4.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs6742301
rs6742301
LINC01127
1 2 101969429 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs150946191
rs150946191
IL1R1
1 2 102116028 intron variant T/G snv 1.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs10409243
rs10409243
DNMT1 ; S1PR2
6 19 10222312 3 prime UTR variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1997502
rs1997502
IL1RL2
2 2 102227789 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs56076326
rs56076326
CUX1
1 7 102237515 intron variant C/T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs1420101
rs1420101
IL18R1 ; IL1RL1
8 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 0.800 1.000 1 2009 2009
dbSNP: rs6543119
rs6543119
IL18R1 ; IL1RL1
1 2 102346612 intron variant A/T snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs5833013
rs5833013
IL18R1 ; IL1RL1
2 2 102352407 intron variant -/TA delins 0.700 1.000 1 2016 2016
dbSNP: rs9807989
rs9807989
IL18R1
2 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs34020101
rs34020101
IL18RAP
2 2 102435015 non coding transcript exon variant AA/-;A;AAA delins 0.700 1.000 1 2016 2016
dbSNP: rs113473633
rs113473633
NFKB1
4 1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 0.700 1.000 2 2016 2019