Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs34612342
MUTYH
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 11
rs36053993
MUTYH
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 9
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 6
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 5
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 2
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 2
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 2
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 2
rs12711521
MASP2 ; TARDBP
0.807 0.240 1 11030859 missense variant C/A snv 0.74 0.63 1
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs2073658
USF1
0.882 0.200 1 161040972 intron variant C/T snv 0.21 1
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 1
rs2516839
USF1
0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 1
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 1
rs72550870
MASP2
0.776 0.360 1 11046609 missense variant T/C snv 2.1E-02 2.2E-02 1
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 19
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 18
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 12