Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12210050 0.807 0.040 6 475489 non coding transcript exon variant C/T snv 0.11 8
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 7
rs1024708183 0.925 0.040 19 7909761 missense variant A/G snv 4
rs10754833 0.851 0.040 1 236021631 intron variant T/A;C snv 4
rs1057519805 1.000 0.040 15 66436839 missense variant T/C snv 3
rs1110400 1.000 0.040 16 89919722 missense variant T/C snv 5.6E-03 6.6E-03 3
rs121913371 1.000 0.040 7 140781678 missense variant G/A;T snv 4.0E-06; 8.0E-06 3
rs397507482 0.882 0.040 7 140753386 missense variant A/C snv 3
rs700635 0.925 0.040 2 201288502 3 prime UTR variant C/A snv 0.72 3
rs749496294 0.925 0.040 20 3562435 missense variant G/A snv 1.2E-05 1.4E-05 3
rs766310650 1.000 0.040 6 36677906 5 prime UTR variant T/C snv 6.2E-05 2.1E-05 3
rs1057519702
KIT
1.000 0.040 4 54726020 missense variant T/C snv 2
rs1057519708
KIT
1.000 0.040 4 54728096 missense variant T/A;G snv 2
rs1057519730 1.000 0.040 15 66436786 missense variant T/A;G snv 2
rs1057519731 0.925 0.040 15 66436816 missense variant G/C snv 2
rs1057519804 1.000 0.040 14 104776711 missense variant G/T snv 2
rs1057519808 1.000 0.040 19 4117543 missense variant T/G snv 2
rs1057519837 1.000 0.040 3 41224631 missense variant C/G;T snv 2
rs1057519856 0.925 0.040 15 66436815 missense variant T/A snv 2
rs1057520031
KIT
1.000 0.040 4 54727440 missense variant A/C;G snv 2
rs11547464 1.000 0.040 16 89919683 missense variant G/A snv 5.3E-03 4.7E-03 2
rs1204552 1.000 0.040 20 36050981 non coding transcript exon variant T/A;C;G snv 2
rs121909233 1.000 0.040 10 87864524 missense variant G/A snv 2
rs121913323 1.000 0.040 19 1220416 stop gained C/T snv 2
rs121913368 0.925 0.040 7 140753345 missense variant AG/GA mnv 2