Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 1
rs6728440 2 19799585 intergenic variant G/A snv 0.89 1
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 7
rs786870
APBB1IP
10 26485765 intron variant T/C snv 0.81 1
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs2427832 1 159263285 intergenic variant A/G snv 0.81 1
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs2494261 1 159281504 upstream gene variant G/A snv 0.80 1
rs2494258 1 159264789 intergenic variant T/C snv 0.80 1
rs2518569
AIM2
1 159125785 intron variant T/G snv 0.80 1
rs2427824
FCER1A
1.000 0.040 1 159295272 intron variant T/C snv 0.79 1
rs2427825
FCER1A
1 159296276 intron variant T/C snv 0.79 1
rs863011 1 159224382 intergenic variant C/T snv 0.79 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs2491204
ARG1
6 131476264 intron variant T/A snv 0.75 1
rs9321294
ARG1
6 131474417 intron variant T/C snv 0.75 1
rs2608928 6 131470731 upstream gene variant A/C snv 0.75 1
rs2608935 6 131468596 upstream gene variant A/G snv 0.75 1
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs2258844 12 121050569 downstream gene variant G/C snv 0.73 1
rs11065385
HNF1A
12 120985583 intron variant A/G snv 0.72 1
rs2649999
HNF1A-AS1
12 120942741 intron variant T/C snv 0.70 1
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7