Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042821
MSH6
0.732 0.280 2 47783349 missense variant G/A;C;T snv 0.18; 8.6E-06 16
rs104894194
AIP
0.925 11 67483198 stop gained C/T snv 2.8E-05 2.1E-05 4
rs10505476
PCAT1 ; POU5F1B ; CASC8
8 127395871 intron variant C/T snv 0.38 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057517457
MUTYH
0.851 0.120 1 45332804 frameshift variant GCCAGCCCAG/- delins 7.0E-06 6
rs1060503115
PMS2
0.763 0.400 7 5978664 missense variant T/A;G snv 13
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs10808555
PCAT1 ; POU5F1B ; CASC8
0.925 0.080 8 127397266 intron variant G/A snv 0.65 6
rs10941112
AMACR ; C1QTNF3-AMACR
0.882 0.120 5 34004602 missense variant C/T snv 0.42 0.38 4
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 11
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1201299
TBL1XR1
3 177053096 intron variant C/T snv 1.7E-02 1
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908874
TSHR ; LOC101928462
0.807 0.080 14 81143584 missense variant T/C snv 7
rs121912532
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.776 0.280 2 48688065 missense variant C/A;G;T snv 1.2E-05 12
rs121912535
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.827 0.240 2 48688427 missense variant A/C snv 6
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14