Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs6461992
HOXA10-HOXA9 ; HOXA11 ; HOXA10
1.000 0.120 7 27181212 3 prime UTR variant A/G snv 0.93 4
rs4722675
HOTTIP
7 27204343 intron variant A/G snv 0.93 4
rs3735533
HOTTIP
7 27206274 non coding transcript exon variant T/C snv 0.93 4
rs6565174
LOC101928595
16 30100583 intron variant A/C snv 0.93 2
rs4551692
PAX2
10 100796696 intron variant G/A snv 0.91 2
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs2023843
HOTTIP
7 27203602 intron variant C/T snv 0.90 2
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs2999159
MOV10
1 112688136 intron variant A/G snv 0.85 4
rs72704264
CD160
1 145721780 intron variant G/C snv 0.85 1
rs4834735
SYNPO2
4 119037654 3 prime UTR variant T/C snv 0.85 1
rs342989 7 35428286 intergenic variant A/G snv 0.84 1
rs2881854
ENPEP
4 110422107 intron variant C/A snv 0.83 2
rs6551716 4 62709978 regulatory region variant T/A snv 0.83 1
rs7592578
NEMP2 ; LOC105376748
2 190574865 regulatory region variant T/G snv 0.83 1
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs1215469
LOC105370275
13 80133273 intron variant A/C snv 0.82 1
rs3745318
KLF2
1.000 0.080 19 16325451 missense variant T/C snv 0.75 0.82 1
rs284844
WBP1L
10 102794772 intron variant A/G snv 0.82 3
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs1250259
FN1 ; LOC105373868
1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs4757391
SOX6
11 16281393 intron variant C/T snv 0.78 2
rs9971406
SOX6
11 16256743 intron variant G/T snv 0.78 1