Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71 5
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 4
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 4
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 3
rs77641731
ABO
1.000 0.040 9 133257521 missense variant T/C snv 3
rs8176719
ABO
0.925 0.120 9 133257521 frameshift variant -/C ins 0.37 0.35 3
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 3
rs3027012
CADM3-AS1 ; ACKR1
1 159204333 5 prime UTR variant C/T snv 0.13 3
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 3
rs9939973
FTO
1.000 0.080 16 53766656 intron variant G/A snv 0.42 3
rs10759944
PTCSC2
0.925 0.080 9 97794690 intron variant A/G snv 0.72 3
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 3
rs7850258
PTCSC2
0.827 0.200 9 97786731 intron variant A/G snv 0.72 3
rs3741298
ZPR1
11 116786845 intron variant C/T snv 0.73 3