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: rs14158
rs14158
LDLR
5 0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 0.010 1.000 1 2013 2013
dbSNP: rs919266
rs919266
BST2
1 19 17403506 intron variant T/C;G snv 0.010 1.000 1 2016 2016
dbSNP: rs6467710
rs6467710
DGKI
1 7 137519073 intron variant G/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs10484554
rs10484554
HLA-B ; LOC112267902
11 0.807 0.200 6 31306778 intron variant C/T snv 0.12 0.800 1.000 1 2009 2009
dbSNP: rs12198173
rs12198173
TNXB
9 0.827 0.240 6 32059031 intron variant G/A snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs1233579
rs1233579 		3 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs1235162
rs1235162
GABBR1
6 0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs13194504
rs13194504 		3 0.925 0.120 6 28662914 intergenic variant G/A snv 5.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2019 2019
dbSNP: rs2248462
rs2248462 		10 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs2284178
rs2284178
HCP5
6 0.925 0.120 6 31464348 non coding transcript exon variant C/T snv 0.44 0.700 1.000 1 2009 2009
dbSNP: rs2395029
rs2395029
HCP5
12 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 0.800 1.000 1 2009 2009
dbSNP: rs241447
rs241447
TAP2
11 0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 0.010 1.000 1 2020 2020
dbSNP: rs2516509
rs2516509
MICB-DT
7 0.882 0.160 6 31482217 intron variant T/C snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs2844511
rs2844511 		10 0.807 0.200 6 31422007 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2844513
rs2844513 		6 0.925 0.120 6 31420437 intron variant G/A snv 0.53 0.700 1.000 1 2009 2009
dbSNP: rs2894207
rs2894207
HLA-B ; LINC02571
8 0.882 0.160 6 31295974 intron variant T/C snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs3093662
rs3093662
TNF
9 0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs3117143
rs3117143
LOC100129636
4 0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs3130380
rs3130380
HCG18 ; HCG17
10 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs3131093
rs3131093 		3 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs3749971
rs3749971
OR5V1 ; OR12D3
4 0.925 0.160 6 29374998 missense variant G/A snv 5.5E-02 5.7E-02 0.700 1.000 1 2009 2009
dbSNP: rs3815087
rs3815087
PSORS1C1
8 0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 0.700 1.000 1 2009 2009
dbSNP: rs3823418
rs3823418
PSORS1C1
8 0.925 0.120 6 31133165 intron variant G/A snv 0.23 0.700 1.000 1 2009 2009
dbSNP: rs4324798
rs4324798 		8 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 0.700 1.000 1 2009 2009