Source: ALL
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
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs3219466
MUTYH ; TOE1
0.851 0.080 1 45340381 5 prime UTR variant G/A;T snv 4
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs7574920
XDH
0.882 0.080 2 31362783 intron variant G/C snv 0.42 3
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs730882035
VHL
0.807 0.200 3 10149805 missense variant G/A snv 7
rs699473
SOD3
0.827 0.160 4 24795181 intron variant C/T snv 0.54 5
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs121918347
SMO
0.851 0.080 7 129210500 missense variant G/T snv 4
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs3731249
CDKN2A
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 23
rs1329443726
CDKN2A
1.000 0.080 9 21971097 frameshift variant C/- delins 1
rs1475218156
CDKN2B ; CDKN2B-AS1
1.000 0.080 9 22006096 missense variant C/G;T snv 4.2E-06; 8.4E-06 1
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 7
rs9420907
STN1
0.790 0.320 10 103916707 intron variant C/A;G snv 7
rs11012732
MLLT10
0.882 0.080 10 21541175 intron variant A/G snv 0.31 5