Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 1
rs1406948
UQCC1
20 35317816 intron variant G/A snv 0.44 1
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 2
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 2
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 1
rs505102
CFH
1 196650372 upstream gene variant T/C snv 0.40 1
rs2076529
TSBP1-AS1 ; BTNL2
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 2
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs7637773
IGF2BP2
1.000 0.080 3 185797847 intron variant G/A snv 0.38 1
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs620861
PCAT1 ; CASC8 ; POU5F1B ; CASC21
0.925 0.080 8 127323428 intron variant G/A snv 0.36 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs1254319
C14orf39
1.000 14 60437039 missense variant G/A snv 0.35 0.36 1
rs7246865
MYO9B
19 17108295 intron variant G/A snv 0.36 1
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 1
rs4640244
KCNJ12
17 21380911 intron variant A/G snv 0.33 1
rs4580892 6 127088737 intron variant C/T snv 0.32 1
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32 1
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2