Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 5
rs6544713
ABCG8
0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 5
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 4
rs2301753
RNF39
0.925 0.040 6 30071463 missense variant G/T snv 0.18 0.17 4
rs611917
CELSR2
1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32 4
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 3
rs16844401
HGFAC
1.000 0.040 4 3447925 missense variant G/A;T snv 7.5E-02; 8.3E-06 3
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 3
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 3
rs1800787
FGB
1.000 0.040 4 154562863 upstream gene variant C/T snv 0.17 3
rs1800789
FGB
1.000 0.040 4 154561591 upstream gene variant G/A snv 0.17 3
rs2281719
GALNT2
1.000 0.040 1 230161913 intron variant C/T snv 0.45 3
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 3
rs255052
DPEP2 ; DUS2
0.925 0.040 16 67991092 intron variant G/A snv 0.17 0.17 3
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 3
rs2865531
CFDP1
1.000 0.040 16 75356418 intron variant T/A snv 0.52 3
rs2967605
RAB11B
0.925 0.040 19 8404854 downstream gene variant C/T snv 0.20 3
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 3
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 3
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 3
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 3
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 3