Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 3
rs11628318 14 102573750 regulatory region variant T/A;C snv 1
rs13042885 20 1944061 upstream gene variant C/A;T snv 1
rs1719271 15 64891602 intron variant A/G snv 0.20 1
rs17568628 5 76751114 intergenic variant T/C;G snv 1
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 1
rs397969 17 19900934 upstream gene variant T/C snv 0.41 1
rs409801 9 4744743 intron variant T/C snv 0.38 1
rs7149242 14 100693079 intergenic variant T/G snv 0.62 1
rs7616006 3 12226148 intergenic variant A/G snv 0.48 1
rs7694379 1.000 4 87265357 intron variant G/A snv 0.40 1
rs4148441
ABCC4
13 95245953 intron variant A/G snv 0.91 1
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 2
rs6490294
ACAD10
12 111752634 intron variant C/A snv 0.35 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 2
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 2
rs1034566
ARVCF
22 19996754 intron variant C/G;T snv 1
rs477895
BAD ; GPR137
11 64281440 intron variant C/T snv 0.74 1
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 2
rs941207
BAZ2A
12 56629500 intron variant C/G snv 0.20 1
rs11602954
BET1L
11 202856 intron variant G/A snv 0.17 2
rs11789898
BRD3
9 134060541 intron variant G/T snv 0.14 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1