Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 3
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs10116277
CDKN2B-AS1
0.827 0.160 9 22081398 intron variant G/T snv 0.62 5
rs10217586
CDKN2B-AS1
1.000 0.040 9 22121350 intron variant A/T snv 0.52 2
rs10218795
HJV
1.000 0.040 1 146018957 intron variant G/A snv 0.15 1
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
rs10431335 1.000 0.040 12 128194523 upstream gene variant C/A;T snv 1
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs10484404
ZNF165 ; ZSCAN16-AS1
1.000 0.040 6 28087717 intron variant C/T snv 0.15 1
rs10498725
CARMIL1
1.000 0.040 6 25454787 intron variant C/T snv 0.17 3
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
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
rs10738606
CDKN2B-AS1
1.000 0.040 9 22088091 intron variant A/T snv 0.42 1
rs10738609
CDKN2B-AS1
1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
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
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 3
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs10757275
CDKN2B-AS1
1.000 0.040 9 22106226 intron variant G/A;T snv 1