Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1041569
TNFSF13B
1.000 0.120 13 108267195 intron variant T/A;C snv 1
rs9611280
TNRC6B
1.000 0.120 22 40156115 missense variant G/A;T snv 6.8E-02; 5.1E-06 1
rs1064796681
TP53
1.000 0.120 17 7675091 missense variant C/T snv 1
rs1036935 0.925 0.120 18 50317164 upstream gene variant A/G;T snv 2
rs1359742 0.925 0.120 9 22336997 intergenic variant G/C;T snv 2
rs1476569 0.925 0.120 4 113777540 intergenic variant A/G snv 0.34 2
rs2511713 0.925 0.120 8 102565637 downstream gene variant A/G snv 0.25 2
rs2511714 0.925 0.120 8 102566646 regulatory region variant T/G snv 0.41 2
rs391023 0.925 0.120 16 85894208 upstream gene variant C/T snv 0.48 2
rs391855 0.925 0.120 16 85895015 upstream gene variant A/T snv 0.52 2
rs4368253 0.925 0.120 18 59955055 TF binding site variant T/A;C snv 2
rs57214277 0.925 0.120 4 184333619 downstream gene variant C/T snv 0.33 2
rs674313 0.925 0.120 6 32610305 intergenic variant C/T snv 0.29 2
rs7169431 0.925 0.200 15 56048698 intergenic variant A/G;T snv 2
rs7254272 0.925 0.120 19 4069121 upstream gene variant G/A snv 0.31 2
rs77551289 0.925 0.120 18 63121512 downstream gene variant A/G snv 6.0E-02 2
rs7944004 0.925 0.120 11 2289922 intergenic variant T/G snv 0.48 2
rs8024033 0.925 0.120 15 40111456 upstream gene variant C/G snv 0.50 2
rs9271176 0.925 0.120 6 32610350 intergenic variant A/G snv 0.69 2
rs13401811
ACOXL
0.925 0.120 2 110858527 intron variant G/A snv 0.19 2
rs1439287
ACOXL-AS1 ; ACOXL ; MIR4435-2HG
0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42 2
rs58055674
ACOXL ; MIR4435-2HG
0.925 0.120 2 111074216 intron variant T/C snv 0.13 2
rs1373425060
AK3
0.925 0.120 9 4719290 missense variant G/C snv 4.0E-06 2
rs71597109
BANK1
0.925 0.120 4 101819845 intron variant C/T snv 0.27 2
rs4987855
BCL2
0.925 0.120 18 63126316 3 prime UTR variant C/T snv 5.9E-02 2