Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 6
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 1
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 5
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 8
rs10774214
CCND2-AS1
0.790 0.080 12 4259186 intron variant T/C snv 0.54 1
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 9
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 18
rs11064437
SPSB2
0.790 0.080 12 6872998 splice acceptor variant C/T snv 9.3E-02 1
rs11169552
ATF1
0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 2
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 10
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 3
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 3
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 51
rs11571658
BRCA2
0.851 0.240 13 32340630 frameshift variant TT/- del 2.8E-05 1
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 31
rs11874392
SMAD7
0.763 0.080 18 48926786 intron variant A/T snv 0.50 2
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 2
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 11
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 8
rs1254244346
ABCA1
1.000 0.080 9 104822502 missense variant G/A snv 4.0E-06 1
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 11