Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25406
PCNA-AS1 ; PCNA
0.807 0.120 20 5118990 intron variant G/A snv 0.41 8
rs267606541
AIP
0.827 0.160 11 67487147 stop gained C/T snv 5
rs2686876 0.882 0.080 11 258909 intergenic variant T/A;C snv 3
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs3219466
MUTYH ; TOE1
0.851 0.080 1 45340381 5 prime UTR variant G/A;T snv 4
rs3731249
CDKN2A
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 23
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15 13
rs587776563
NF2
1.000 0.080 22 29668440 frameshift variant A/- delins 1
rs603965
CCND1
0.732 0.440 11 69648142 splice region variant G/A snv 14
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699473
SOD3
0.827 0.160 4 24795181 intron variant C/T snv 0.54 5
rs730882035
VHL
0.807 0.200 3 10149805 missense variant G/A snv 7
rs7574920
XDH
0.882 0.080 2 31362783 intron variant G/C snv 0.42 3
rs768803947
TP53
0.882 0.080 17 7670624 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs9420907
STN1
0.790 0.320 10 103916707 intron variant C/A;G snv 7