Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs6495314
CHRNB4 ; LOC112268142
0.925 0.080 15 78668187 intron variant A/C snv 0.35 3
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 3
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 6
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs3130893 0.882 0.160 6 29012930 intergenic variant A/G snv 5.3E-02 3
rs8038920
CHRNB4 ; LOC112268142
0.925 0.080 15 78682203 intron variant A/G snv 0.62 3
rs259940
ZNRD1ASP
0.925 0.080 6 30044157 intron variant A/G snv 0.23 2
rs3885951
HYKK
1.000 0.040 15 78533575 missense variant A/G snv 7.5E-02 6.9E-02 2
rs2495239
FOXP4-AS1
1.000 0.040 6 41522750 intron variant A/G snv 0.84 1
rs1316971
CHRNB4
0.925 0.080 15 78638168 intron variant A/G;T snv 0.62 3
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs3117143
LOC100129636
0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 4
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 4
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2
rs10519198
IREB2
0.925 0.080 15 78450412 intron variant C/A;G snv 2
rs11638372
LOC112268142 ; CHRNB4
0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 3
rs9480192
LOC105378054
1.000 0.040 6 150305155 intergenic variant C/A;G;T snv 1