Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 118
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 42
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 32
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs121913254
NRAS
0.658 0.440 1 114713909 stop gained G/A;C;T snv 29
rs36053993
MUTYH
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 24
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 17
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 14
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 13
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 7
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 6
rs10754833
NID1
0.851 0.040 1 236021631 intron variant T/A;C snv 4
rs1232547491
RHCE
0.851 0.120 1 25385838 missense variant A/G snv 4
rs3219466
MUTYH ; TOE1
0.851 0.080 1 45340381 5 prime UTR variant G/A;T snv 4
rs4845618
IL6R
0.851 0.160 1 154427539 intron variant G/T snv 0.53 4
rs746830376
EPHB2
0.925 0.200 1 22784501 missense variant G/A snv 2.4E-05 3.5E-05 4
rs781734330
ATP13A2
0.851 0.080 1 16995981 missense variant C/T snv 4
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3
rs529365517
FLVCR1 ; FLVCR1-DT
0.925 0.080 1 212858540 missense variant C/T snv 3