Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2420371
F5
1 169522317 intron variant G/A snv 0.95 4
rs4911499 20 35419819 intergenic variant C/T snv 0.95 2
rs224334
GDF5
20 35436939 intron variant A/G snv 0.92 2
rs224330
GDF5-AS1 ; GDF5
20 35434398 synonymous variant T/C snv 0.90 2
rs224320 20 35422754 intergenic variant G/A snv 0.88 2
rs334152
IWS1
2 127491865 intron variant C/T snv 0.87 2
rs334138
IWS1
2 127514892 non coding transcript exon variant A/G snv 0.87 2
rs819168 20 34316039 upstream gene variant T/G snv 0.87 2
rs819156
AHCY
20 34293217 intron variant A/C snv 0.87 2
rs777569
LOC105373608 ; IWS1
2 127471572 intron variant A/T snv 0.87 2
rs2679409
IWS1
2 127512533 intron variant C/T snv 0.87 2
rs819131 20 34320043 intergenic variant G/A snv 0.87 2
rs1019842
MYO7B
2 127547621 intron variant T/C snv 0.86 2
rs9287540
MYO7B
2 127540151 intron variant T/G snv 0.86 2
rs843901 20 34316830 intergenic variant T/G snv 0.86 2
rs2163348
MYO7B
2 127541503 intron variant A/G snv 0.86 2
rs819167 20 34315881 upstream gene variant A/G snv 0.85 2
rs777554
IWS1
2 127521471 intron variant C/A snv 0.85 2
rs7582598 2 127532280 upstream gene variant G/A snv 0.84 2
rs334143
IWS1
2 127505900 intron variant C/T snv 0.82 2
rs6060488
FER1L4
20 35585256 non coding transcript exon variant A/G snv 0.80 0.80 2
rs2298308
SOGA1
20 36784431 3 prime UTR variant G/A snv 0.80 2
rs4663109 2 127164716 intergenic variant A/G snv 0.78 2
rs6738690 2 127235149 intergenic variant T/C snv 0.77 2
rs6430936 2 127250110 downstream gene variant A/C snv 0.77 2