Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs745564626
XRCC3 ; KLC1
0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05 14
rs861530
LOC112268131 ; XRCC3 ; KLC1
0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs1799794
XRCC3 ; KLC1
0.763 0.320 14 103712930 splice region variant T/C snv 0.22 12
rs1297812518
LOC112268131 ; KLC1 ; XRCC3
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05 9
rs1799796
XRCC3 ; KLC1
0.790 0.240 14 103699590 intron variant T/A;C snv 0.31 7
rs28903081
KLC1 ; XRCC3
0.851 0.200 14 103698934 missense variant C/A;T snv 4.5E-06; 4.3E-04 5
rs768891111
XRCC3 ; KLC1
0.851 0.080 14 103699474 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 4
rs77381814
KLC1 ; XRCC3
0.882 0.080 14 103699410 missense variant C/T snv 1.5E-03 5.9E-03 3
rs709399
XRCC3 ; KLC1 ; LOC112268131
0.882 0.080 14 103701208 3 prime UTR variant G/A snv 0.59 0.61 3
rs861531
XRCC3 ; LOC112268131 ; KLC1
0.882 0.120 14 103706470 3 prime UTR variant C/A snv 0.32 3
rs1360602468
KLC1 ; XRCC3
0.925 0.080 14 103698904 missense variant G/C;T snv 2
rs149642280
KLC1 ; XRCC3
14 103699501 missense variant C/T snv 1.0E-04; 4.0E-06 3.5E-05 2
rs3212057
LOC112268131 ; XRCC3 ; KLC1
0.925 0.080 14 103707128 missense variant C/T snv 1.4E-03 6.3E-03 2
rs3212121
XRCC3 ; KLC1
14 103698185 3 prime UTR variant T/C snv 1.9E-02 2
rs45603942
XRCC3 ; KLC1
0.925 0.080 14 103712895 5 prime UTR variant G/A snv 1.2E-04 2
rs861529
XRCC3 ; KLC1
0.925 0.080 14 103712977 3 prime UTR variant T/C snv 0.91 2
rs861528
XRCC3 ; ZFYVE21
0.925 0.080 14 103716661 intron variant C/T snv 0.17 2
rs546983534
KLC1 ; XRCC3 ; LOC112268131
14 103708630 missense variant G/A snv 2.8E-05 1
rs861536
LOC112268131 ; XRCC3 ; KLC1
14 103701227 3 prime UTR variant A/G snv 0.28 0.30 1
rs3212112
XRCC3 ; KLC1
1.000 0.040 14 103699345 intron variant A/C snv 7.1E-03 2.2E-02 1
rs861537
XRCC3 ; KLC1 ; LOC112268131
1.000 0.080 14 103700738 intron variant C/T snv 0.61 0.61 1
rs1178552124
XRCC3 ; LOC112268131 ; KLC1
1.000 0.040 14 103703253 synonymous variant G/A snv 1
rs3212079
XRCC3 ; LOC112268131 ; KLC1
1.000 0.080 14 103704128 3 prime UTR variant G/A snv 5.2E-02 1