Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 4
rs116480994
ZNRD1
0.925 0.080 6 30064745 3 prime UTR variant A/C snv 2
rs7042889 0.925 0.080 9 129033082 upstream gene variant A/C snv 0.15 2
rs116260619 1.000 0.080 6 30479897 intergenic variant A/C snv 1
rs55902839
TMEM237
1.000 0.080 2 201641266 intron variant A/C snv 0.47 1
rs67340775
ZSCAN31
1.000 0.080 6 28336607 intron variant A/C snv 6.3E-02 1
rs77045810 1.000 0.080 1 168535779 downstream gene variant A/C snv 0.10 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 3
rs2596500
HLA-B
0.925 0.120 6 31353490 intron variant A/C;G snv 2
rs35755165 0.882 0.080 19 40840084 intron variant A/C;G snv 2
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 4
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs722864
MAP3K20
0.882 0.080 2 173118476 intron variant A/C;G;T snv 1
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs8042059
CHRNA3
0.882 0.080 15 78615517 intron variant A/C;T snv 2
rs12901682
PSMA4
0.851 0.200 15 78540881 5 prime UTR variant A/C;T snv 1
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 1
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 17
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 11
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 10