Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs4851527
IL1R2
0.790 0.160 2 102005914 intron variant A/G snv 0.63 7
rs719250
IL1R2
0.827 0.200 2 102007256 intron variant C/T snv 0.11 5
rs3218896
IL1R2
0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs77381814
KLC1 ; XRCC3
0.882 0.080 14 103699410 missense variant C/T snv 1.5E-03 5.9E-03 3
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs2255336
LOC101928100 ; KLRK1 ; KLRC4-KLRK1
0.827 0.200 12 10379727 missense variant T/C snv 0.81 0.74 5
rs807181
PSMD10 ; ATG4A
0.851 0.120 X 108090354 intron variant G/C;T snv 4
rs807183
ATG4A
0.851 0.120 X 108094263 intron variant G/A snv 0.51 4
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1143630
IL1B
0.827 0.160 2 112834078 intron variant T/A;G snv 5
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs997271472
APC
1.000 0.080 5 112838434 missense variant G/A;T snv 4.0E-06 1
rs864622584
APC
1.000 0.080 5 112838623 missense variant G/A snv 1
rs1110839
PAX8-AS1 ; PAX8
0.807 0.120 2 113236840 non coding transcript exon variant G/A;C;T snv 6
rs4848320
PAX8 ; PAX8-AS1
0.807 0.120 2 113253214 intron variant C/G;T snv 6
rs4570
UTP23 ; RAD21
0.882 0.080 8 116846150 3 prime UTR variant G/A snv 0.70 4
rs2289937
RAD21
0.882 0.080 8 116861572 intron variant G/A;C snv 4
rs4579555
RAD21
0.882 0.080 8 116867092 intron variant A/G snv 4
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28