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
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24 13
rs3917225
IL1R1
0.807 0.160 2 102152842 intron variant A/G snv 0.36 6
rs2227869
ERCC5 ; BIVM-ERCC5
0.790 0.240 13 102862735 missense variant G/A;C snv 4.3E-02 9
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs768891111
XRCC3 ; KLC1
0.851 0.080 14 103699474 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 4
rs709399
XRCC3 ; KLC1 ; LOC112268131
0.882 0.080 14 103701208 3 prime UTR variant G/A snv 0.59 0.61 3
rs1297812518
LOC112268131 ; KLC1 ; XRCC3
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05 9
rs861530
LOC112268131 ; XRCC3 ; KLC1
0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs34677591
SDHD ; TIMM8B
0.742 0.120 11 112086941 missense variant G/A snv 7.5E-03 7.0E-03 12
rs11214077
SDHD ; TIMM8B
0.752 0.120 11 112087953 missense variant A/G snv 6.6E-03 6.7E-03 12
rs360717
IL18
0.851 0.080 11 112164002 5 prime UTR variant G/A snv 0.25 4
rs360718
IL18
0.827 0.120 11 112164016 5 prime UTR variant A/C snv 0.26 5
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1946519
IL18
0.851 0.120 11 112164784 intron variant A/C snv 0.60 4
rs3783521
IL1A
0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 8
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs200817352
PAX8 ; PAX8-AS1
1.000 0.080 2 113220126 missense variant G/A;C snv 2.0E-03; 4.0E-06 2
rs78201625
HABP2
0.851 0.080 10 113577182 missense variant C/T snv 2.4E-03 1.8E-03 4
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31