Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6963345
ZKSCAN1
7 100020983 intron variant G/A;C snv 1
rs2067832
STN1
10 103883376 intron variant G/A snv 0.44 1
rs1980653
STN1
10 103894406 intron variant A/G snv 0.44 1
rs11191865
STN1
0.925 0.160 10 103913084 intron variant G/A snv 0.44 3
rs10902073 11 1060934 TF binding site variant C/A snv 0.31 1
rs10794278 11 1061718 intergenic variant G/T snv 0.32 1
rs10794279 11 1061781 intergenic variant C/T snv 0.32 1
rs10794280 11 1062867 intergenic variant C/T snv 0.30 1
rs10751635 11 1062990 intergenic variant A/G snv 0.41 1
rs2301160 11 1063767 intergenic variant T/C snv 0.41 1
rs10794284 11 1067011 intergenic variant G/A snv 0.34 1
rs7942850
LOC107987157
11 1068900 intergenic variant T/C snv 0.36 1
rs2071174
MUC2 ; LOC107987157
11 1073712 upstream gene variant T/C snv 0.39 1
rs7396030
MUC2
11 1085368 intron variant A/G snv 0.71 1
rs10902088
MUC2
1.000 0.040 11 1090036 non coding transcript exon variant T/C snv 0.73 2
rs7934606
MUC2
1.000 0.040 11 1100037 intron variant C/G;T snv 2
rs6421972
MUC2
11 1102586 synonymous variant C/T snv 0.30 1
rs7480563
MUC2
11 1107741 non coding transcript exon variant T/C snv 0.58 0.56 1
rs4077759 11 1112068 downstream gene variant C/T snv 0.53 1
rs1278769
ATP11A
13 112882313 3 prime UTR variant A/G snv 0.77 1
rs7005380
DEPTOR
8 119941633 intron variant G/A;C snv 1
rs2672794 1.000 0.040 11 1219775 intron variant T/C snv 0.70 2
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 14
rs868903
MUC5B
0.882 0.120 11 1221460 upstream gene variant T/C snv 0.47 4
rs2672812
MUC5B
11 1228142 intron variant G/A snv 0.51 1