Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
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
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 4
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 4
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 4
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 4
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 3
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 3
rs181937009
LOC107986652 ; LOC100507477
0.925 0.040 6 140064258 intron variant A/G snv 0.23 3
rs12290663 0.925 0.040 11 26141193 intergenic variant G/A snv 5.7E-02 2