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: rs12339348
rs12339348
IL33 ; LOC107987046
2 1.000 0.080 9 6233082 intron variant A/G;T snv 0.800 1.000 2 2013 2018
dbSNP: rs17294280
rs17294280
SMAD3
4 0.882 0.120 15 67175947 intron variant A/G snv 0.19 0.800 1.000 2 2013 2016
dbSNP: rs34290285
rs34290285
D2HGDH
8 0.851 0.120 2 241759225 intron variant G/A snv 0.27 0.700 1.000 2 2017 2018
dbSNP: rs367023
rs367023
LINC00299
2 1.000 0.040 2 8309993 intron variant A/G snv 0.35 0.800 1.000 2 2013 2016
dbSNP: rs4795400
rs4795400
GSDMB
3 0.925 0.080 17 39910767 intron variant C/T snv 0.36 0.800 1.000 2 2013 2016
dbSNP: rs61839660
rs61839660
IL2RA
9 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 0.700 1.000 2 2017 2018
dbSNP: rs7824394
rs7824394 		1 8 80380364 intron variant A/C;T snv 0.700 1.000 2 2016 2017
dbSNP: rs869402
rs869402
GSDMB
3 0.925 0.160 17 39911790 intron variant T/A;C snv 0.800 1.000 2 2013 2018
dbSNP: rs950881
rs950881
IL18R1 ; IL1RL1
2 1.000 0.120 2 102316052 intron variant G/A;T snv 0.800 1.000 2 2013 2016
dbSNP: rs10033073
rs10033073
STX18-AS1 ; LOC101928279
1 4 4773674 intron variant A/G snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs10038058
rs10038058
WDR36
1 5 111107582 intron variant A/G snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs10038177
rs10038177
WDR36
3 0.925 0.040 5 111100751 intron variant C/T snv 0.53 0.54 0.700 1.000 1 2013 2013
dbSNP: rs10041894
rs10041894 		1 5 40493132 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10043301
rs10043301
TTC33
1 5 40530784 intron variant C/T snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs10045255
rs10045255
WDR36
1 5 111102658 intron variant A/G snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs10051830
rs10051830
WDR36
1 5 111117147 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10055177
rs10055177
WDR36
1 5 111114886 intron variant T/G snv 0.53 0.700 1.000 1 2013 2013
dbSNP: rs10055860
rs10055860
TTC33
1 5 40569851 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10060003
rs10060003
WDR36
1 5 111113658 intron variant A/G snv 0.53 0.700 1.000 1 2013 2013
dbSNP: rs10068204
rs10068204
TTC33
1 5 40519249 intron variant T/C snv 0.63 0.700 1.000 1 2013 2013
dbSNP: rs10068717
rs10068717
NDFIP1
1 5 142115369 intron variant C/T snv 0.67 0.700 1.000 1 2017 2017
dbSNP: rs10074523
rs10074523
KIF3A
2 1.000 0.080 5 132724891 intron variant C/A snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs10075020
rs10075020
TTC33
1 5 40575737 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10076944
rs10076944 		1 5 40496849 intron variant G/A snv 0.60 0.700 1.000 1 2013 2013
dbSNP: rs1008723
rs1008723
GSDMB
3 0.925 0.160 17 39910014 intron variant G/C;T snv 0.700 1.000 1 2013 2013