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: rs869312892
rs869312892
STAT3
3 0.925 0.120 17 42316899 missense variant G/A snv 0.800 1.000 3 2014 2017
dbSNP: rs587777648
rs587777648
STAT3
2 0.925 0.120 17 42329612 missense variant T/C snv 0.800 1.000 2 2014 2017
dbSNP: rs587777649
rs587777649
STAT3
1 1.000 17 42322445 missense variant G/A;C snv 4.0E-06 0.800 1.000 2 2014 2017
dbSNP: rs587777650
rs587777650
STAT3
1 1.000 17 42322409 missense variant C/G snv 0.800 1.000 2 2014 2017
dbSNP: rs706778
rs706778
IL2RA
19 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 2 2015 2019
dbSNP: rs10202630
rs10202630 		4 0.882 2 190398199 intergenic variant T/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs1032129
rs1032129
TNFRSF11B
5 0.851 0.040 8 118939661 intron variant A/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs10425559
rs10425559 		7 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs10444776
rs10444776
LOC112268138
4 0.882 14 105647030 upstream gene variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10494079
rs10494079
VAV3
4 0.882 1 107832253 intron variant G/C snv 9.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs10748781
rs10748781 		11 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10797431
rs10797431
LOC100996583
5 0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs10822050
rs10822050 		14 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs10937560
rs10937560
MB21D2
4 0.882 3 192909627 intron variant G/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10986284
rs10986284 		4 0.882 9 124236874 intergenic variant A/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10988542
rs10988542
FNBP1
14 0.724 0.240 9 129894985 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs11073337
rs11073337
RASGRP1
5 0.851 0.040 15 38555562 intron variant A/C snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs11086102
rs11086102 		6 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs11117433
rs11117433 		6 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11145763
rs11145763
CARD9
14 0.724 0.240 9 136369144 intron variant A/C;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs114378220
rs114378220
CAMK4
5 0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs114558062
rs114558062 		5 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 0.700 1.000 1 2019 2019
dbSNP: rs114846446
rs114846446
LINC01250
14 0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
14 0.724 0.240 1 67203951 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs11622435
rs11622435
LOC101928462
7 0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 0.700 1.000 1 2019 2019