Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519725
KRAS
0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06 6
rs1057519822
MAP2K1
0.925 0.080 15 66481818 missense variant T/A snv 3
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1060503118
PMS2
0.925 0.080 7 5987422 missense variant C/T snv 2
rs1064795841
TP53
0.882 0.080 17 7674971 missense variant C/T snv 4
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs10774214
CCND2-AS1
0.790 0.080 12 4259186 intron variant T/C snv 0.54 9
rs1078643
TMEM220-AS1 ; TMEM238L
0.776 0.080 17 10803924 missense variant G/A;C snv 10
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs10849432
LOC105369625
0.790 0.080 12 6276561 intergenic variant C/T snv 0.84 9
rs10849433
LOC105369624
0.776 0.080 12 6297738 regulatory region variant T/C snv 0.38 10
rs10849438 0.790 0.080 12 6302870 intergenic variant T/G snv 1.0E-01 9
rs10904849
CUBN
0.790 0.080 10 16955267 intron variant G/A;T snv 0.25 9
rs10911251
LAMC1
0.790 0.080 1 183112059 intron variant A/C snv 0.37 9
rs10934578
CASR
0.925 0.080 3 122258435 intron variant G/T snv 0.30 4
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs10951878 0.790 0.080 7 46887097 downstream gene variant C/A;T snv 9
rs10958713
IKBKB
0.925 0.080 8 42323198 intron variant C/T snv 0.28 2
rs10980628
LPAR1
0.776 0.080 9 110909123 intron variant T/C snv 0.16 10
rs11064437
SPSB2
0.790 0.080 12 6872998 splice acceptor variant C/T snv 9.3E-02 9
rs11085466
LOC101929007
0.790 0.080 19 21569009 intron variant G/C snv 0.23 10
rs11087784 0.776 0.080 20 7760329 intergenic variant A/G snv 0.13 10
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17