Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 3
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1
rs13314271
TP63
0.925 0.080 3 189639813 intron variant T/C snv 0.45 1
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 1
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 1
rs1903003
FAM13A
0.925 0.080 4 88965146 intron variant C/G;T snv 3
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2
rs12503223
LDB2
1.000 0.040 4 16841093 intron variant G/A snv 0.18 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 4
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 4
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 4
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 1
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47 1
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6