Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075674
TFR2
1.000 0.040 7 100627408 synonymous variant G/A snv 0.18 0.16 1
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 5
rs7801190
SLC12A9
1.000 0.040 7 100860471 non coding transcript exon variant C/G snv 9.9E-02 1
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 2
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 3
rs3824755
CYP17A1
0.925 0.120 10 102836092 intron variant G/A;C;T snv 2
rs12411886
CNNM2
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02 3
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 6
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 3
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 3
rs1165668
TTC41P
1.000 0.040 12 103924218 intron variant G/A snv 0.71 1
rs1165669
TTC41P
1.000 0.040 12 103924394 intron variant A/G snv 0.71 1
rs2385168
LHFPL3
1.000 0.040 7 104438209 intron variant C/A;T snv 0.41 1
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 2
rs2066718
ABCA1
0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 2
rs2515629
ABCA1
1.000 0.040 9 104832083 intron variant A/G snv 0.16 3
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2
rs4149268
ABCA1
1.000 0.040 9 104884939 intron variant C/T snv 0.46 4
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 4
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs11112992
POLR3B
1.000 0.040 12 106435501 intron variant T/C snv 0.20 1
rs342293
CTB-30L5.1
0.882 0.040 7 106731773 intron variant C/G snv 0.42 1
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 1
rs11671653
DNM2
1.000 0.040 19 10727810 intron variant G/A;T snv 1