Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750547
MLH1
0.925 0.160 3 37020312 stop gained T/C;G snv 4.0E-06 3
rs63751701
EPM2AIP1 ; MLH1
0.925 0.080 3 36993663 stop gained G/A;T snv 3
rs748676559
ACACA
0.925 0.080 17 37284932 missense variant C/T snv 4.0E-06 2.1E-05 3
rs760891242
XPC
0.925 0.080 3 14168309 missense variant G/C snv 4.0E-06 7.0E-06 3
rs774904310
CDKN2A
0.925 0.080 9 21971055 frameshift variant C/- delins 3
rs869312770
MSH6 ; FBXO11
0.925 0.160 2 47800829 frameshift variant AG/- delins 3
rs886063150
CA2
0.925 0.080 8 85477151 missense variant C/A;T snv 8.0E-06 3
rs9869263
LOC107986170 ; CLDN1
0.925 0.080 3 190312891 synonymous variant A/C;G;T snv 8.0E-06; 0.83; 4.0E-06 3
rs10450310
MBL2
0.925 0.080 10 52764898 downstream gene variant G/A snv 0.29 2
rs1060503118
PMS2
0.925 0.080 7 5987422 missense variant C/T snv 2
rs10958713
IKBKB
0.925 0.080 8 42323198 intron variant C/T snv 0.28 2
rs11625206
MAP3K9
0.925 0.080 14 70727436 3 prime UTR variant C/T snv 0.26 2
rs11832059
VDR
0.925 0.080 12 47879066 missense variant A/C;G snv 4.0E-06; 1.9E-03 2
rs11923427
RAF1
0.925 0.080 3 12622336 intron variant C/G;T snv 2
rs119490107
FSBP ; RAD54B
0.925 0.080 8 94399540 missense variant C/A snv 2.8E-05 2
rs121434507
PTPRJ
0.925 0.080 11 48123636 missense variant C/T snv 4.0E-05 6.3E-05 2
rs121434623
PTPN12
0.925 0.080 7 77571160 missense variant A/G snv 2
rs121909242
PPARG
0.925 0.080 3 12416825 missense variant A/C snv 2
rs1238788540
BRAF
0.925 0.080 7 140800368 missense variant G/C snv 4.0E-06 7.0E-06 2
rs12485716
CASR
0.925 0.080 3 122260843 intron variant G/A snv 0.36 2
rs12490683
LOC105377207 ; MYLKP1
0.925 0.080 3 75329934 non coding transcript exon variant G/A snv 0.46 2
rs12497343
MYLKP1 ; LOC105377207
0.925 0.080 3 75330074 intron variant C/G;T snv 2
rs1287152741
DHFR
0.925 0.080 5 80633984 missense variant C/T snv 8.0E-06 1.4E-05 2
rs1323151304
POLE
0.925 0.080 12 132643933 frameshift variant TA/- delins 2
rs1365611 0.925 0.080 4 174462542 intergenic variant C/T snv 0.28 2