Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 3
rs10068737 5 118700852 intergenic variant T/A;C snv 1
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 1
rs12575381 11 135033566 regulatory region variant G/A snv 0.16 1
rs16864170 1.000 0.080 2 5767748 intergenic variant T/C snv 3.8E-02 1
rs1933182 1.000 0.080 1 109457216 intergenic variant A/C snv 0.63 1
rs2453533 1.000 0.080 15 45349027 intergenic variant C/A snv 0.56 1
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 1
rs2880072 6 159404417 downstream gene variant G/A snv 0.49 1
rs2887915 2 210689850 intergenic variant C/G;T snv 1
rs500456 7 54531089 intergenic variant A/G snv 0.47 1
rs6465825 1.000 0.080 7 77787122 downstream gene variant T/C snv 0.41 1
rs3764913
ACADL
1.000 0.080 2 210210185 non coding transcript exon variant T/C snv 0.30 0.27 1
rs2014355
ACADS
0.925 0.120 12 120737721 non coding transcript exon variant T/C snv 0.22 1
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 1
rs6546837
ALMS1
2 73450771 missense variant G/C;T snv 0.27 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 3
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 3
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 3
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7