Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63406760
CDK2AP1 ; C12orf65
1.000 0.120 12 123258146 intron variant G/- delins 0.63 2
rs6898653 0.925 0.120 5 116639960 intergenic variant A/G snv 0.26 2
rs7328203
LINC02341
1.000 0.120 13 42414410 intron variant T/G snv 0.48 2
rs7758579 0.925 0.120 6 52221483 TF binding site variant G/A snv 0.25 2
rs887864
CLEC16A
0.925 0.120 16 11065028 intron variant G/A;C;T snv 2
rs950881
IL18R1 ; IL1RL1
1.000 0.120 2 102316052 intron variant G/A;T snv 2
rs10124907 1.000 0.120 9 25659639 intergenic variant A/G;T snv 1
rs10156309
NKAIN3
1.000 0.120 8 62520233 intron variant C/T snv 4.6E-02 1
rs11027293 1.000 0.120 11 23530907 intergenic variant T/G snv 2.4E-02 1
rs111371454
RTF1
1.000 0.120 15 41468419 intron variant A/G snv 0.34 1
rs11256017 1.000 0.120 10 9001956 intergenic variant T/A;C snv 1
rs11668618
MRPL4
1.000 0.120 19 10255220 non coding transcript exon variant C/T snv 0.16 1
rs11671925
SLC7A10
1.000 0.120 19 33227147 upstream gene variant G/A snv 0.21 1
rs11677002
FOSL2 ; FLJ31356
1.000 0.120 2 28391534 intron variant T/C snv 0.39 1
rs11680788
LINC00486
1.000 0.120 2 32834029 intron variant C/T snv 6.3E-02 1
rs12509403
NFKB1 ; LOC105377347
1.000 0.120 4 102604193 intron variant C/T snv 0.31 1
rs12520745
LINC02240 ; LOC101927421
1.000 0.120 5 125252697 intron variant C/T snv 0.18 1
rs12597084
RBFOX1
1.000 0.120 16 5769619 intron variant A/C snv 0.67 1
rs12939457
ZPBP2
1.000 0.120 17 39875935 intron variant T/C snv 0.38 1
rs12973620 1.000 0.120 19 57738275 intron variant G/C snv 0.16 1
rs1332366 1.000 0.120 9 75217659 intergenic variant G/A snv 0.15 1
rs1352323
ST8SIA2
1.000 0.120 15 92452411 intron variant G/A snv 0.32 1
rs1373976132
HNMT
1.000 0.120 2 137964586 missense variant T/C snv 4.0E-06 1
rs138050288
RERE
1.000 0.120 1 8400188 intron variant CA/- del 0.22 1
rs141023293
SIK3
1.000 0.120 11 116902201 intron variant G/A snv 1.5E-02 1