Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11990063
MSRA
0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs1961982
C12orf42
0.925 0.040 12 103218955 intergenic variant G/A snv 0.27 2
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs10884216
LINC02627
0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs35792458
XKR6
0.925 0.040 8 10964921 intron variant G/C snv 0.53 3
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 3
rs17158930
DOCK4
0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3
rs139459337
ZBTB20
0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs10809520 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 2
rs10233018 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 2
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 2
rs760161369
MTHFR
0.882 0.040 1 11800214 missense variant G/A;C snv 2.8E-05; 4.0E-06 1
rs2017122
KMT2A
0.925 0.040 11 118444134 intron variant C/T snv 4.0E-02 2
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs7189979
SNX29
0.925 0.040 16 12536330 intron variant A/C;G;T snv 3
rs11728985
C4orf33
0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs2221540
OPCML
0.925 0.040 11 132846474 intron variant A/G snv 0.11 2
rs201569130 0.925 0.040 6 1402916 intergenic variant GACA/- delins 1.1E-02 3
rs142484554
SPSB4
0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs11155372
UTRN
0.925 0.040 6 144698602 intron variant G/C;T snv 3
rs9321987
UTRN
0.925 0.040 6 144709148 intron variant C/T snv 0.40 3