Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1032841
LINC01814
1.000 0.040 2 8526108 intron variant A/G;T snv 1
rs10468514 1.000 0.040 17 45378874 intergenic variant A/G snv 0.38 1
rs10489854 1.000 0.040 1 159279069 non coding transcript exon variant C/T snv 8.3E-02 1
rs10756796
BNC2
1.000 0.040 9 16730976 intron variant A/G snv 0.43 1
rs10822037
ZNF365
1.000 0.040 10 62616798 intron variant T/C snv 0.71 1
rs10937319
RTP2 ; LOC100131635
1.000 0.040 3 187711669 intron variant T/A;C snv 1
rs10991797
LINC00484
1.000 0.040 9 91168389 intron variant A/G snv 0.71 1
rs111267073 1.000 0.040 5 111030094 intergenic variant C/T snv 1.9E-02 1
rs11213941 1.000 0.040 11 111563369 downstream gene variant T/C snv 0.35 1
rs11265449
SLAMF1
1.000 0.040 1 160612458 intron variant C/G snv 0.45 0.36 1
rs11466681
TNFRSF18
1.000 0.040 1 1206007 intron variant C/T snv 6.1E-02 1
rs114997373 1.000 0.040 1 45535906 downstream gene variant G/A snv 1.2E-02 1
rs115390301
OTUD7B
1.000 0.040 1 149981477 intron variant G/A snv 1.1E-02 1
rs11626205
RIN3
1.000 0.040 14 92558117 intron variant G/A snv 0.28 1
rs11736191
LOC101928279 ; STX18-AS1
1.000 0.040 4 4766748 intron variant T/G snv 0.54 1
rs11783015
CCDC26
1.000 0.040 8 128682763 intron variant T/C snv 0.23 1
rs118013485 1.000 0.040 19 33235671 TF binding site variant G/A snv 5.0E-02 1
rs11916411
UBE2E2
1.000 0.040 3 23526489 intron variant A/C;T snv 1
rs1201113
TNFRSF8
1.000 0.040 1 12084377 intron variant G/A snv 0.16 1
rs12068304
BATF3
1.000 0.040 1 212691650 intron variant A/G snv 0.20 1
rs12152276
NRROS ; PIGX
1.000 0.040 3 196641630 intron variant A/G snv 5.7E-02 1
rs12185242
ZNF652
1.000 0.040 17 49329709 intron variant A/C snv 0.38 1
rs12282231 1.000 0.040 11 2274398 upstream gene variant C/T snv 9.0E-02 1
rs12303699
PLXNC1
1.000 0.040 12 94188560 intron variant G/A snv 0.30 1
rs1260294
PITPNM2
1.000 0.040 12 123075742 5 prime UTR variant T/A;C snv 1