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: rs12365699
rs12365699 		5 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 0.700 1.000 2 2019 2019
dbSNP: rs12964116
rs12964116
SERPINB7
2 0.925 0.080 18 63775385 5 prime UTR variant A/G snv 3.0E-02 0.700 1.000 2 2019 2019
dbSNP: rs13277355
rs13277355 		3 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 0.700 1.000 2 2019 2019
dbSNP: rs16903574
rs16903574
OTULINL
6 0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 0.700 1.000 2 2019 2019
dbSNP: rs1837253
rs1837253 		10 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 0.700 1.000 2 2019 2019
dbSNP: rs1887704
rs1887704
UBAC2
2 0.925 0.080 13 99322238 intron variant C/G snv 0.55 0.700 1.000 2 2019 2019
dbSNP: rs2066844
rs2066844
NOD2
54 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 0.700 1.000 2 2019 2019
dbSNP: rs3122929
rs3122929
STAT6
4 0.882 0.080 12 57115319 intron variant C/T snv 0.33 0.700 1.000 2 2019 2019
dbSNP: rs34290285
rs34290285
D2HGDH
8 0.851 0.120 2 241759225 intron variant G/A snv 0.27 0.700 1.000 2 2019 2019
dbSNP: rs35570272
rs35570272
GLB1
2 0.925 0.080 3 33006170 intron variant G/T snv 0.36 0.700 1.000 2 2019 2019
dbSNP: rs3785356
rs3785356
IL4R
5 0.925 0.080 16 27337847 intron variant C/T snv 0.25 0.700 1.000 2 2019 2019
dbSNP: rs4574025
rs4574025
TNFRSF11A
4 0.882 0.160 18 62342581 intron variant C/T snv 0.55 0.700 1.000 2 2019 2019
dbSNP: rs4795399
rs4795399
GSDMB
2 0.925 0.080 17 39905186 intron variant T/C snv 0.35 0.700 1.000 2 2019 2019
dbSNP: rs5743618
rs5743618
TLR1
25 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 0.700 1.000 2 2019 2019
dbSNP: rs62623446
rs62623446
TESPA1
3 0.882 0.120 12 54974507 missense variant C/T snv 4.5E-02 4.4E-02 0.700 1.000 2 2019 2019
dbSNP: rs72823641
rs72823641
IL18R1 ; IL1RL1
4 0.882 0.080 2 102319699 intron variant T/A;C snv 0.700 1.000 2 2019 2019
dbSNP: rs928413
rs928413
IL33
7 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 0.700 1.000 2 2014 2019
dbSNP: rs9391997
rs9391997
IRF4
4 0.851 0.160 6 409119 3 prime UTR variant A/G snv 0.38 0.700 1.000 2 2019 2019
dbSNP: rs943451
rs943451
PRKCQ ; PRKCQ-AS1
2 0.925 0.080 10 6579811 intron variant T/C snv 0.51 0.700 1.000 2 2019 2019
dbSNP: rs10036789
rs10036789 		3 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10158467
rs10158467 		2 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10175070
rs10175070
CCL20
1 1.000 0.080 2 227805859 5 prime UTR variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10187276
rs10187276 		2 0.925 0.080 2 227805721 upstream gene variant T/C snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs10208293
rs10208293
IL18R1 ; IL1RL1
4 0.882 0.160 2 102349850 intron variant G/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10414065
rs10414065 		4 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 0.700 1.000 1 2019 2019