Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7640677 3 48340996 intergenic variant G/A snv 1.2E-02 1
rs10041590
C5orf17
5 24064827 intron variant T/C;G snv 2
rs10054178
C5orf17
5 24059742 intron variant A/G snv 7.5E-02 2
rs10056373
C5orf17
5 24069684 intron variant C/T snv 7.4E-02 2
rs113051092
C5orf17
5 24060490 intron variant A/T snv 7.4E-02 2
rs16893073
C5orf17
5 24072508 intron variant C/G;T snv 2
rs73055009
C5orf17
5 24058406 intron variant A/G snv 7.5E-02 2
rs73055087
C5orf17
5 24062454 intron variant C/A;T snv 2
rs79056512
C5orf17
5 24063287 intron variant G/A snv 7.4E-02 2
rs4359426
CCL22
0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94 3
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3091250
CCR3
1.000 0.040 3 46264639 non coding transcript exon variant G/T snv 0.26 2
rs183662584
CCR5 ; CCR5AS
1.000 3 46373218 missense variant G/A snv 5.2E-04 1.5E-04 2
rs1800452
CCR5AS ; CCR5
3 46373570 missense variant G/A snv 4.9E-03 1.9E-03 1
rs765009973
CCR5AS ; CCR5
3 46373909 missense variant G/T snv 7.4E-05 2.1E-05 1
rs2853699
CCR8
3 39332411 missense variant C/A;G;T snv 4.0E-06; 0.21; 2.8E-05 1
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 8
rs2255301
CD4
0.925 0.160 12 6800276 intron variant T/C snv 0.59 0.61 3
rs10892961
CLMP
11 123093392 intron variant A/C;G;T snv 2
rs11218976
CLMP
11 123090950 intron variant A/G snv 0.41 2
rs7109445
CLMP
11 123094779 intron variant A/C;G snv 2
rs7121616
CLMP
11 123095918 intron variant A/G snv 0.41 2
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs2907092
CTNND2
5 11047569 intron variant T/A;G snv 1
rs2586052
CUEDC1
17 57885718 5 prime UTR variant A/G;T snv 1