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: rs5742909
rs5742909
CTLA4
40 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 0.010 1.000 1 2017 2017
dbSNP: rs1051336
rs1051336
HLA-DRA
2 0.925 0.120 6 32444815 3 prime UTR variant G/A;C snv 0.15 0.010 1.000 1 2018 2018
dbSNP: rs11218708
rs11218708 		1 1.000 0.080 11 122601355 regulatory region variant G/A snv 0.19 0.710 1.000 1 2018 2018
dbSNP: rs28483633
rs28483633 		1 1.000 0.080 6 32657097 upstream gene variant C/A snv 2.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs7454108
rs7454108 		2 0.925 0.120 6 32713706 upstream gene variant T/C snv 9.1E-02 0.710 1.000 1 2018 2018
dbSNP: rs1074532
rs1074532 		1 1.000 0.080 4 65791342 intergenic variant A/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs17315309
rs17315309
ST18
1 1.000 0.080 8 52295127 intron variant A/G;T snv 0.12 0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
IL1A
43 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 0.010 1.000 1 2019 2019
dbSNP: rs28362491
rs28362491
NFKB1 ; LOC105377621
56 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2019 2019
dbSNP: rs361525
rs361525
TNF
62 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2019 2019
dbSNP: rs4073
rs4073
CXCL8
64 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2019 2019
dbSNP: rs70993900
rs70993900 		3 0.882 0.080 6 32618381 intergenic variant C/- delins 4.8E-02 0.710 1.000 1 2019 2019
dbSNP: rs9469220
rs9469220 		5 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 0.710 1.000 1 2019 2019
dbSNP: rs1800872
rs1800872
IL10 ; IL19
119 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2020 2020