Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11428092
USP34
1.000 0.040 2 61301164 intron variant -/A delins 0.34 1
rs17524488
SPP1
0.925 0.040 4 87975555 non coding transcript exon variant -/G delins 4
rs2239704
LTA ; LOC100287329
0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64 17
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs10775412
KSR1
0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs1551399
LOC105375746
0.827 0.120 8 125527723 intron variant A/C snv 0.46 5
rs61802846
FCGR2A
0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 5
rs422544 0.925 0.120 6 33058333 regulatory region variant A/C snv 0.30 2
rs68177277
LOC107984669 ; GPR65
1.000 0.040 14 88008109 intron variant A/C snv 0.12 1
rs8088140
HRH4
1.000 0.040 18 24469176 intron variant A/C snv 0.66 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs2227981
LOC105373977 ; PDCD1
0.763 0.400 2 241851121 synonymous variant A/C;G snv 1.6E-04; 0.63 12
rs714830
CDKAL1
0.827 0.120 6 20624151 intron variant A/C;G snv 0.13 5
rs7195296 0.827 0.120 16 11655918 intergenic variant A/C;G snv 5
rs2857151 0.925 0.160 6 32795737 intergenic variant A/C;G snv 2
rs1009759
PDCD1LG2
1.000 0.040 9 5556786 intron variant A/C;G snv 1
rs11062385
KDM5A
1.000 0.040 12 318409 missense variant A/C;G snv 1.2E-05; 0.31 1
rs148783236
LOC107984741 ; USP8
1.000 0.040 15 50492819 missense variant A/C;G snv 2.5E-03 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs4149570
TNFRSF1A
0.752 0.360 12 6342424 upstream gene variant A/C;G;T snv 11
rs4672505 0.827 0.120 2 62333197 regulatory region variant A/C;G;T snv 5