Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6531565
RELL1
4 37660910 intron variant T/A snv 0.99 2
rs1741629 20 23918358 downstream gene variant G/T snv 0.96 2
rs7675915
STX18-AS1
4 4677180 intron variant A/G snv 0.96 2
rs1392502
APOOP5
16 59753666 intron variant T/G snv 0.89 2
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 1
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5
rs822531 7 148932667 intergenic variant C/T snv 0.85 3
rs204664 20 552161 intergenic variant G/A snv 0.83 2
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 2
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 2
rs4239436
CABLES1
18 23151966 intron variant A/G snv 0.81 3
rs3101457
C1orf100
1 244369912 intron variant G/A snv 0.80 1
rs1776897 6 34227234 regulatory region variant G/T snv 0.80 3
rs3897379 1 219586391 regulatory region variant A/G snv 0.79 2
rs9920506
CHRNB4
15 78638715 intron variant A/G snv 0.79 1
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs2656071
IREB2
15 78453001 intron variant T/A snv 0.79 1
rs2568488
IREB2
15 78444251 intron variant T/A snv 0.78 1
rs924840
IREB2
15 78439466 intron variant T/A snv 0.78 1
rs2869045 15 78426557 regulatory region variant T/C snv 0.78 2
rs1106529
TBX15
1 118988874 intron variant G/A snv 0.77 3
rs215607
PDE1C
7 32298725 missense variant G/A snv 0.79 0.77 1
rs589428
SLC44A4 ; CYP21A2 ; EHMT2 ; LOC107986588 ; EHMT2-AS1
1.000 0.120 6 31880443 non coding transcript exon variant T/G snv 0.77 2
rs7166081 0.925 0.080 15 67199963 downstream gene variant G/A snv 0.76 4
rs8102683 19 40857860 intron variant T/C snv 0.75 1