Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 3
rs11072811
MORF4L1
1.000 0.040 15 78839988 intron variant A/C snv 0.51 1
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 1
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 1
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs2246942
LIPA
0.925 0.040 10 89245129 intron variant A/C;G snv 1
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 2
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 5
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 3
rs1004638
CDKN2B-AS1
1.000 0.040 9 22115590 intron variant A/C;T snv 2
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 1
rs9316753 1.000 0.040 13 54893794 intergenic variant A/C;T snv 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6