Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs766812
CCDC26
1.000 0.080 8 128992458 intron variant A/G snv 0.91 1
rs7018275
CCDC26
1.000 0.080 8 129004253 intron variant C/T snv 0.90 1
rs1372452
CCDC26
1.000 0.080 8 129016788 intron variant A/G snv 0.90 1
rs12334809
CCDC26
1.000 0.080 8 129018760 non coding transcript exon variant T/C snv 0.88 1
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs861020
IRF6
1.000 0.080 1 209803766 intron variant A/G snv 0.82 1
rs1038294
COL8A1
0.925 0.120 3 99784884 intron variant A/G snv 0.82 2
rs5763674
MTMR3
0.925 0.120 22 29990369 non coding transcript exon variant C/T snv 0.78 2
rs1243572 0.925 0.120 14 94913162 intergenic variant T/C snv 0.78 2
rs6995235
CCDC26
1.000 0.080 8 128941690 intron variant A/G snv 0.77 1
rs1519850
CCDC26
1.000 0.080 8 128884575 intron variant C/T snv 0.77 1
rs493760
DROSHA
0.851 0.200 5 31436933 intron variant C/T snv 0.74 5
rs4752028
SHTN1
0.807 0.200 10 117075480 intron variant C/T snv 0.73 6
rs10956453
CCDC26
1.000 0.080 8 128937545 intron variant G/C snv 0.72 1
rs1850889
CCDC26
1.000 0.080 8 128878159 intron variant A/G snv 0.72 1
rs287982 0.925 0.120 2 9832313 regulatory region variant C/T snv 0.70 2
rs7815713
CCDC26
1.000 0.080 8 128883227 intron variant T/C snv 0.69 1
rs2485893 1.000 0.080 1 210174810 downstream gene variant A/G snv 0.68 1
rs68092024
CMSS1 ; FILIP1L
0.925 0.120 3 99972678 intron variant C/T snv 0.68 2
rs12543318 0.882 0.120 8 87856112 intergenic variant C/A snv 0.68 4
rs6029228
LOC102724968
1.000 0.080 20 40626908 intergenic variant T/G snv 0.68 1
rs6585429
VAX1
0.925 0.120 10 117133720 3 prime UTR variant A/G snv 0.68 2
rs6102074
LOC102724968
1.000 0.080 20 40639545 regulatory region variant G/T snv 0.67 2
rs7015145
CCDC26
1.000 0.080 8 128697039 intron variant A/G snv 0.67 1
rs6102085 1.000 0.080 20 40652989 intergenic variant G/A snv 0.66 1