Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs919266
BST2
19 17403506 intron variant T/C;G snv 1
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs241447
TAP2
0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 11
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 8
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 8
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs7756521
DDR1
1.000 6 30880476 intron variant T/C snv 0.25 5
rs1369619997
KIDINS220
2 8731746 missense variant G/C snv 4.0E-06 1
rs4118325 1 107035210 intergenic variant G/A;T snv 1
rs6467710
DGKI
7 137519073 intron variant G/A;C snv 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 8
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 8
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6
rs527476195
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 6
rs14158
LDLR
0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5