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: 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: rs3132461
rs3132461 		1 1.000 0.080 6 31512891 upstream gene variant G/A snv 0.84 0.700 1.000 1 2017 2017
dbSNP: rs408014
rs408014
TXNDC5 ; BLOC1S5-TXNDC5
1 1.000 0.080 6 7899161 intron variant G/A snv 0.31 0.010 1.000 1 2017 2017
dbSNP: rs4396968
rs4396968
GABRB1
1 1.000 0.080 4 47087167 intron variant T/C snv 0.85 0.700 1.000 1 2017 2017
dbSNP: rs55859133
rs55859133
MAPK3
1 1.000 0.080 16 30116944 missense variant C/T snv 1.7E-03 1.4E-03 0.010 1.000 1 2016 2016
dbSNP: rs59661306
rs59661306
ADGRV1 ; LUCAT1
1 1.000 0.080 5 91087644 intron variant A/G snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs6547598
rs6547598
TCF7L1
1 1.000 0.080 2 85219363 intron variant A/G snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs6812281
rs6812281 		1 1.000 0.080 4 179391655 intron variant T/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs73730372
rs73730372 		1 1.000 0.080 6 32616804 regulatory region variant C/T snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs7457728
rs7457728
LINC01445
1 1.000 0.080 7 54380269 intron variant G/C snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs7771314
rs7771314
TXNDC5 ; BLOC1S5-TXNDC5
1 1.000 0.080 6 7891170 intron variant T/C snv 9.3E-02 0.010 1.000 1 2017 2017
dbSNP: rs9532669
rs9532669 		1 1.000 0.080 13 40927414 downstream gene variant A/T snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs17102999
rs17102999
MLH3
2 0.925 0.120 14 75046831 missense variant G/A snv 1.3E-02 9.8E-03 0.010 1.000 1 2014 2014
dbSNP: rs997363
rs997363
C2orf83
2 0.925 0.080 2 227644742 intron variant C/T snv 0.64 0.700 1.000 1 2014 2014
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: 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: 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: 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: 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: 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: 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