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: rs11071559
rs11071559
RORA
4 0.925 0.080 15 60777789 intron variant C/T snv 0.23 0.700 1.000 2 2019 2019
dbSNP: rs12023876
rs12023876
ADORA1
2 0.925 0.080 1 203124073 intron variant G/A;T snv 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: 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: 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: 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: rs4790522
rs4790522
TRPV1
2 0.925 0.080 17 3566559 3 prime UTR variant A/C snv 0.55 0.020 1.000 2 2015 2015
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: 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: rs8069176
rs8069176 		4 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 0.800 1.000 2 2007 2018
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: rs10044254
rs10044254
FBXL7
2 0.925 0.080 5 15783487 intron variant A/G snv 0.25 0.010 1.000 1 2014 2014
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: 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
dbSNP: rs10494132
rs10494132
CHIA
4 0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 0.010 1.000 1 2017 2017
dbSNP: rs10519031
rs10519031 		1 1.000 0.080 15 59890806 regulatory region variant T/C snv 2.2E-02 0.010 1.000 1 2015 2015
dbSNP: rs10830123
rs10830123
NPS
1 1.000 0.080 10 127551386 intron variant G/C snv 0.29 0.010 1.000 1 2017 2017
dbSNP: rs10836538
rs10836538
PRR5L
2 0.925 0.080 11 36343703 intron variant G/T snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs10924993
rs10924993 		2 0.925 0.080 1 236296485 intergenic variant T/A;G snv 0.700 1.000 1 2007 2007
dbSNP: rs11000019
rs11000019
PSAP
1 1.000 0.080 10 71831773 intron variant G/A snv 3.3E-02 0.800 1.000 1 2013 2013
dbSNP: rs11021111
rs11021111 		1 1.000 0.080 11 95270099 intergenic variant C/G snv 4.3E-02 0.700 1.000 1 2013 2013