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: rs10004195
rs10004195
TLR10
8 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs10008492
rs10008492 		2 1.000 0.120 4 38764099 intergenic variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10024216
rs10024216 		1 4 38762491 upstream gene variant G/A snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs10034903
rs10034903
TLR10
1 4 38783057 upstream gene variant C/G snv 0.35 0.700 1.000 1 2013 2013
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: rs10056340
rs10056340 		3 0.925 0.080 5 110854353 intergenic variant T/G snv 0.31 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: 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
dbSNP: rs10114457
rs10114457 		1 9 6130940 intergenic variant A/G snv 0.81 0.700 1.000 1 2013 2013
dbSNP: rs10166330
rs10166330
IL18RAP
1 2 102433930 intron variant C/T snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs10167431
rs10167431
IL1RL2
1 2 102236342 intron variant T/C snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs10170583
rs10170583
IL18R1
1 2 102358304 intron variant G/A snv 0.45 0.700 1.000 1 2013 2013
dbSNP: rs10172039
rs10172039
IL1R1
1 2 102122325 intron variant C/A snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs10172116
rs10172116 		1 2 102471113 upstream gene variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10173081
rs10173081
IL18R1 ; IL1RL1
2 1.000 0.080 2 102340888 intron variant C/T snv 0.18 0.700 1.000 1 2013 2013