Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 5
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 5
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 5
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 5
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 4
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 4
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 4
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 4
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 4
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs2206277
TFAP2B
0.925 0.080 6 50830813 intron variant C/T snv 0.19 4
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 3
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 3
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 3
rs17410962 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 3
rs17489282 1.000 0.040 8 19995007 regulatory region variant C/T snv 0.25 3