Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10131567 1.000 0.040 14 35395672 intergenic variant G/T snv 0.22 1
rs10244416 1.000 0.040 7 20536128 intergenic variant C/A;T snv 0.52 1
rs10245867
JAZF1
0.925 0.080 7 28102567 intron variant G/T snv 0.37 2
rs10249788
LOC101927609 ; AHR
0.827 0.160 7 17298523 intron variant C/G;T snv 6
rs1025549
PLCL1
1.000 0.040 2 198016459 intron variant G/A;T snv 1
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
rs1050153
TFRC
0.925 0.120 3 196049444 3 prime UTR variant G/A snv 2
rs10519068
RORA
0.925 0.120 15 60776505 intron variant G/A snv 0.22 2
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs1064795104
EXOC6B
0.790 0.440 2 72498492 stop gained A/C snv 17
rs10756796
BNC2
1.000 0.040 9 16730976 intron variant A/G snv 0.43 1
rs10791824
OVOL1-AS1 ; OVOL1
0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs10822037
ZNF365
1.000 0.040 10 62616798 intron variant T/C snv 0.71 1
rs10910095
LOC100996583
1.000 0.040 1 2579316 upstream gene variant G/A;C snv 2
rs10937319
RTP2 ; LOC100131635
1.000 0.040 3 187711669 intron variant T/A;C snv 1
rs10947428
ITPR3
1.000 0.040 6 33679281 intron variant T/C snv 0.26 2
rs10991797
LINC00484
1.000 0.040 9 91168389 intron variant A/G snv 0.71 1
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs11079788
TBX21
0.925 0.120 17 47743357 intron variant C/T snv 0.23 2
rs111267073 1.000 0.040 5 111030094 intergenic variant C/T snv 1.9E-02 1
rs11150780
SLC38A10
0.925 0.120 17 81290360 intron variant A/G;T snv 2
rs11167761
PCDH1
0.925 0.120 5 141858778 intron variant G/A snv 0.14 2