Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10094872
CASC11
0.882 0.200 8 127707639 intron variant A/T snv 0.33 4
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1034925236
NR5A2
0.925 0.120 1 200048258 missense variant G/C snv 2
rs1037189404
MUC1
0.776 0.280 1 155187519 missense variant C/T snv 8
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs104894094
CDKN2A
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 12
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894360
KRAS
0.724 0.560 12 25209904 missense variant T/A;C snv 14
rs1049074086
CTSD
0.925 0.120 11 1759567 missense variant A/G snv 7.0E-06 9
rs10500715
SBF2
0.925 0.120 11 9951515 intron variant T/G snv 0.39 2
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10835188
LIN7C
1.000 0.120 11 27501639 intron variant G/T snv 0.68 2
rs10887710 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 2
rs10919791 0.925 0.240 1 199996040 intergenic variant G/A snv 0.22 2
rs10983614
ASTN2
1.000 0.120 9 117306874 intron variant T/A;C snv 1
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 6
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2