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: rs9272143
rs9272143
HLA-DQA1
3 0.882 0.080 6 32633026 intron variant T/C snv 0.49 0.720 1.000 4 2013 2017
dbSNP: rs13117307
rs13117307
EXOC1
6 0.827 0.080 4 55885574 intron variant C/T snv 0.21 0.720 1.000 3 2013 2017
dbSNP: rs3117027
rs3117027
HLA-DPB2
3 0.882 0.080 6 33121846 intron variant C/A;G snv 0.720 1.000 3 2013 2018
dbSNP: rs9277952
rs9277952 		4 0.851 0.080 6 33236497 upstream gene variant G/A snv 0.10 0.720 1.000 3 2013 2016
dbSNP: rs11079454
rs11079454
BRIP1
3 0.882 0.080 17 61679808 3 prime UTR variant T/A;C snv 0.020 0.500 2 2013 2016
dbSNP: rs1003897973
rs1003897973
TRIP10 ; LOC107985302
3 0.882 0.080 19 6746039 missense variant C/G snv 0.010 < 0.001 1 2002 2002
dbSNP: rs1007541
rs1007541
FSHR
4 0.882 0.080 2 48981895 intron variant C/T snv 0.16 0.010 1.000 1 2017 2017
dbSNP: rs1030389
rs1030389
PWAR6 ; SNHG14
3 0.882 0.080 15 25032641 non coding transcript exon variant A/G snv 0.41 0.010 1.000 1 2016 2016
dbSNP: rs10426502
rs10426502
MYDGF ; TNFAIP8L1
3 0.882 0.080 19 4651257 intron variant G/A snv 6.8E-02 0.010 1.000 1 2019 2019
dbSNP: rs1042725
rs1042725
HMGA2
7 0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 0.010 1.000 1 2016 2016
dbSNP: rs1045935
rs1045935
PWAR6 ; SNHG14
3 0.882 0.080 15 25036439 non coding transcript exon variant G/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs1048512
rs1048512
KCNJ10 ; PIGM
3 0.882 0.080 1 160025108 3 prime UTR variant G/A;T snv 0.13 0.010 1.000 1 2016 2016
dbSNP: rs1060555
rs1060555
MYDGF ; TNFAIP8L1
3 0.882 0.080 19 4652810 3 prime UTR variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs10802996
rs10802996
EXO1
5 0.882 0.080 1 241847325 upstream gene variant C/A;G snv 0.010 1.000 1 2012 2012
dbSNP: rs10815144
rs10815144
JAK2 ; INSL6
3 0.882 0.080 9 5010192 intron variant G/A snv 0.62 0.010 1.000 1 2014 2014
dbSNP: rs10893506
rs10893506
ST3GAL4
5 0.882 0.080 11 126406065 5 prime UTR variant T/A;C snv 6.4E-06; 0.41 0.010 1.000 1 2014 2014
dbSNP: rs11202058
rs11202058
WAPL
3 0.882 0.080 10 86522854 non coding transcript exon variant G/A snv 0.25 0.010 1.000 1 2015 2015
dbSNP: rs115137622
rs115137622
HLA-DPA3 ; HCG24 ; LOC105375021
1 1.000 0.080 6 33143124 intron variant C/G snv 0.700 1.000 1 2019 2019
dbSNP: rs11568785
rs11568785
TGFBR1
5 0.882 0.080 9 99143552 intron variant A/G;T snv 7.2E-02 0.010 1.000 1 2019 2019
dbSNP: rs1195571
rs1195571 		3 0.882 0.080 12 130739483 intergenic variant T/C snv 0.97 0.010 < 0.001 1 2019 2019
dbSNP: rs12349785
rs12349785
JAK2 ; INSL6
3 0.882 0.080 9 5076613 intron variant G/C snv 0.23 0.010 1.000 1 2014 2014
dbSNP: rs12646659
rs12646659
VEGFC
3 0.882 0.080 4 176764117 intron variant C/G snv 5.4E-02 0.010 1.000 1 2019 2019
dbSNP: rs1474348
rs1474348
IL6 ; IL6-AS1
4 0.882 0.080 7 22728289 intron variant C/G snv 0.71 0.010 1.000 1 2017 2017
dbSNP: rs16945692
rs16945692
BRIP1
3 0.882 0.080 17 61862883 intron variant A/G snv 0.17 0.010 1.000 1 2013 2013
dbSNP: rs16970849
rs16970849
TMC8
4 0.882 0.080 17 78137827 intron variant G/A;T snv 0.11; 4.0E-06 0.010 1.000 1 2016 2016