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: rs9963862
rs9963862
RBBP8
1 1.000 0.120 18 23007948 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs9277534
rs9277534
HLA-DPB1
7 0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 0.010 1.000 1 2019 2019
dbSNP: rs9270986
rs9270986
HLA-DRB1
3 0.882 0.160 6 32606283 intergenic variant A/C snv 0.85 0.700 1.000 1 2015 2015
dbSNP: rs9261290
rs9261290
RNF39
10 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 0.700 1.000 1 2012 2012
dbSNP: rs887464
rs887464
POU5F1 ; PSORS1C3
2 0.925 0.200 6 31178143 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs886424
rs886424
LINC00243
10 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs886403
rs886403
MUC21
2 0.925 0.160 6 30989841 3 prime UTR variant T/C snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs8321
rs8321
ZNRD1
16 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs8058696
rs8058696
ABCC6
1 1.000 0.120 16 16185012 synonymous variant G/C;T snv 0.42 0.010 1.000 1 2017 2017
dbSNP: rs8058694
rs8058694
ABCC6
1 1.000 0.120 16 16185006 missense variant G/T snv 0.42 0.43 0.010 1.000 1 2017 2017
dbSNP: rs7775397
rs7775397
TSBP1 ; TSBP1-AS1
7 0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs7762279
rs7762279 		6 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs7750641
rs7750641
TCF19
6 0.807 0.360 6 31161533 missense variant C/T snv 7.0E-02 7.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs7749323
rs7749323 		2 0.925 0.200 6 137909252 intergenic variant G/A snv 3.3E-02 0.010 < 0.001 1 2017 2017
dbSNP: rs7574865
rs7574865
STAT4
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2018 2018
dbSNP: rs733618
rs733618
CTLA4
12 0.763 0.440 2 203866221 upstream gene variant T/C snv 0.10 0.030 0.667 3 2017 2019
dbSNP: rs6998967
rs6998967
LOC105375922
1 1.000 0.120 8 80451970 intron variant G/A snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs6679356
rs6679356
IL12RB2
2 0.925 0.200 1 67354511 intron variant C/T snv 0.75 0.010 1.000 1 2018 2018
dbSNP: rs564353179
rs564353179
TTN ; LOC101927055
1 1.000 0.120 2 178780121 missense variant C/G snv 9.6E-05 9.1E-05 0.010 < 0.001 1 2013 2013
dbSNP: rs558702
rs558702
C2 ; CYP21A2 ; ZBTB12
6 0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs4958881
rs4958881
TNIP1
7 0.827 0.280 5 151070675 intron variant T/C snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs4678
rs4678
VARS2
2 0.925 0.200 6 30926164 missense variant G/A snv 0.14 0.15 0.700 1.000 1 2012 2012
dbSNP: rs4574025
rs4574025
TNFRSF11A
4 0.882 0.160 18 62342581 intron variant C/T snv 0.55 0.700 1.000 1 2016 2016
dbSNP: rs4361859
rs4361859 		1 1.000 0.120 9 97062415 regulatory region variant G/A snv 0.77 0.010 1.000 1 2007 2007
dbSNP: rs4263037
rs4263037
TNFRSF11A
1 1.000 0.120 18 62349000 intron variant G/A snv 0.61 0.700 1.000 1 2015 2015