Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 10
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9