Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 2
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 3
rs1004638
CDKN2B-AS1
1.000 0.040 9 22115590 intron variant A/C;T snv 2
rs10116277
CDKN2B-AS1
0.827 0.160 9 22081398 intron variant G/T snv 0.62 5
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs10456100
KCNK5
1.000 0.040 6 39215694 intron variant C/T snv 0.20 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 1
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42 2
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 3
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 1
rs10755578
LPA
0.925 0.040 6 160548706 intron variant C/G snv 0.44 0.42 1
rs10757264
CDKN2B-AS1
1.000 0.040 9 22019733 intron variant A/G snv 0.58 2
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 2
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 1
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 1
rs10811656
CDKN2B-AS1
0.807 0.200 9 22124473 intron variant C/T snv 0.47 1
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4