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: rs140991990
rs140991990
SOX9-AS1 ; LINC02097
1 1.000 0.080 17 72101710 intron variant A/G snv 5.5E-04 0.010 1.000 1 2020 2020
dbSNP: rs2116260
rs2116260 		1 1.000 0.080 6 33057663 TF binding site variant T/C snv 8.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs3117008
rs3117008
HLA-DPB2
1 1.000 0.080 6 33128497 intron variant G/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs3129275
rs3129275
HLA-DPB2
1 1.000 0.080 6 33126481 intron variant C/T snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs4713607
rs4713607
HLA-DPB2
1 1.000 0.080 6 33123059 intron variant G/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs864622584
rs864622584
APC
1 1.000 0.080 5 112838623 missense variant G/A snv 0.010 < 0.001 1 2005 2005
dbSNP: rs9391756
rs9391756
HCG24
1 1.000 0.080 6 33148017 upstream gene variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs997271472
rs997271472
APC
1 1.000 0.080 5 112838434 missense variant G/A;T snv 4.0E-06 0.010 < 0.001 1 2005 2005
dbSNP: rs929783669
rs929783669
STK11
1 1.000 0.080 19 1220674 missense variant T/C snv 0.700 0
dbSNP: rs3117039
rs3117039
HLA-DPB2
2 0.925 0.160 6 33118074 intron variant C/T snv 0.35 0.700 1.000 1 2013 2013
dbSNP: rs7770370
rs7770370
HLA-DPA1 ; HLA-DPB1
2 0.925 0.160 6 33081144 non coding transcript exon variant A/G snv 0.27 0.700 1.000 1 2013 2013
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: 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: rs9272143
rs9272143
HLA-DQA1
3 0.882 0.080 6 32633026 intron variant T/C snv 0.49 0.720 1.000 3 2013 2014
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
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