Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1041163
VCAM1
0.882 0.160 1 100718269 upstream gene variant T/C snv 0.18 3
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs2305160
NPAS2 ; NPAS2-AS1
0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs4648022
NFKB1
1.000 0.120 4 102575280 intron variant C/A;T snv 1
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1785882
CARD16 ; LOC107984381
1.000 0.120 11 105052348 intron variant A/T snv 0.45 1
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs2582869
TNFSF13B
1.000 0.120 13 108259797 intron variant A/G;T snv 1
rs227060
C11orf65 ; ATM
0.882 0.160 11 108334154 intron variant C/T snv 0.27 3
rs12711521
MASP2 ; TARDBP
0.807 0.240 1 11030859 missense variant C/A snv 0.74 0.63 7
rs3789068
MIR4435-2HG ; BCL2L11
0.925 0.120 2 111151670 intron variant A/G snv 0.41 2
rs2637988
IL1RN
1.000 0.120 2 113119202 intron variant G/A snv 0.53 1
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs9610
IL10RA ; SMIM35
0.882 0.240 11 118001371 3 prime UTR variant G/A;T snv 0.51 4
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6
rs80202369 1.000 0.120 11 118873150 intergenic variant G/A snv 6.6E-03 1
rs1790192
CXCR5
1.000 0.120 11 118886482 non coding transcript exon variant G/A;C snv 0.58 1
rs78440425
CXCR5
1.000 0.120 11 118888302 intron variant G/A snv 1.1E-02 1
rs2509049
H2AX
0.827 0.160 11 119095811 upstream gene variant C/A;T snv 6
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs16917496
KMT5A
0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21