Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 8
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 6
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 5
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 5
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 3
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 3
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 3
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 2
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 2
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 2