Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17007417 0.882 0.080 2 71808541 regulatory region variant T/C snv 0.85 3
rs171915
LOC153910
1.000 0.080 6 142545708 intron variant G/A snv 0.22 3
rs2293035
XRCC1
0.882 0.080 19 43546923 synonymous variant G/A snv 1.6E-04 1.5E-04 3
rs2830581
ADAMTS5
1.000 0.080 21 26921481 3 prime UTR variant G/A;C snv 3
rs4646421
CYP1A1
0.882 0.080 15 74723851 intron variant G/A;C;T snv 0.21 3
rs66904256
ABCB4
0.882 0.080 7 87439777 missense variant T/A snv 3
rs6940552
ZNRD1ASP
1.000 0.080 6 30044563 intron variant G/A snv 0.12 3
rs750814369
FAM89B ; ZNRD2-AS1 ; ZNRD2
1.000 0.080 11 65570617 missense variant C/A;T snv 2.8E-05 3
rs80291436
VCX
1.000 0.080 X 7843706 missense variant T/A;C;G snv 4.9E-05; 0.19 3
rs886039463
PTPN11
1.000 0.080 12 112489096 missense variant C/A snv 3
rs1012335
IFNAR1
0.925 0.080 21 33341701 intron variant G/C;T snv 2
rs1014509103
ADAMTS4
1.000 0.080 1 161194005 missense variant G/A snv 4.0E-06 2.8E-05 2
rs1053133
BYSL
1.000 0.080 6 41932887 3 prime UTR variant C/A;T snv 2
rs1065205
SERPINB11 ; SERPINB3
1.000 0.080 18 63655761 missense variant T/C;G snv 0.15 2
rs121913675
MET
0.925 0.080 7 116778953 missense variant C/T snv 2
rs121913677
MET
0.925 0.080 7 116783402 missense variant A/G snv 2
rs12427129
HOTAIR ; HOXC11
1.000 0.080 12 53973906 missense variant C/T snv 9.0E-02 7.0E-02 2
rs12438080
CERS3
1.000 0.080 15 100541858 intron variant A/C snv 0.50 2
rs17084733
KIT
1.000 0.080 4 54738774 3 prime UTR variant G/A snv 0.10 2
rs1713449
TEP1
1.000 0.080 14 20373548 missense variant C/T snv 0.26 0.29 2
rs17427960
HOTTIP
0.925 0.080 7 27202847 intron variant C/A snv 2
rs17501292
HOTTIP ; HOXA13
1.000 0.080 7 27201854 non coding transcript exon variant T/C;G snv 2
rs2118593
RYBP
1.000 0.080 3 72447740 upstream gene variant G/A;C;T snv 2
rs2118610
SMAD3
1.000 0.080 15 67135996 intron variant T/C snv 0.59 2
rs2148356 1.000 0.080 9 7395038 intergenic variant G/A;C snv 2