Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 10
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs527476195
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 6
rs1369619997
KIDINS220
2 8731746 missense variant G/C snv 4.0E-06 1
rs374596032
KIDINS220
2 8813255 missense variant A/C;G snv 4.0E-06; 8.0E-06 1
rs4118325 1 107035210 intergenic variant G/A;T snv 1
rs6467710
DGKI
7 137519073 intron variant G/A;C snv 1
rs919266
BST2
19 17403506 intron variant T/C;G snv 1
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 8
rs13194504 0.925 0.120 6 28662914 intergenic variant G/A snv 5.1E-02 3
rs3117143
LOC100129636
0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 4
rs3749971
OR12D3 ; OR5V1
0.925 0.160 6 29374998 missense variant G/A snv 5.5E-02 5.7E-02 4
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 9
rs3131093 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 3
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs1233579 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 3
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9