Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37 4
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3
rs8170
BABAM1 ; USHBP1
0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 3
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 3
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 3
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 3
rs3218020
CDKN2B-AS1
0.882 0.120 9 21997873 intron variant G/A;C snv 3
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 3
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 3
rs2725207
PKD2
0.882 0.200 4 88058377 intron variant C/A snv 0.31 3
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 3
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 3
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs4148323
UGT1A10 ; UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A8 ; UGT1A1 ; UGT1A4
0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 3
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 2