Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11761528
ZKSCAN5
1.000 0.120 7 99521178 intron variant C/T snv 0.12 2
rs740160
ARPC1A
1.000 0.120 7 99360257 intron variant C/T snv 8.6E-02 1
rs111988552
TSPAN5
1.000 0.120 4 98557163 intron variant A/T snv 1
rs2274795
PAPOLA
1.000 0.120 14 96528345 intron variant T/C snv 0.26 1
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 3
rs11121380
SPSB1
1.000 0.120 1 9348900 intron variant A/C snv 0.11 1
rs4272
CDK6
1.000 0.120 7 92607515 3 prime UTR variant A/G;T snv 2
rs9909240
LOC105371532 ; NTN1
1.000 0.120 17 9236774 intron variant G/A snv 0.50 1
rs7164176 1.000 0.120 15 91668544 intergenic variant G/A snv 0.65 1
rs6496667
ZNF774 ; GABARAPL3
1.000 0.120 15 90350436 upstream gene variant C/A;G;T snv 1
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 1
rs8041687
ISG20
1.000 0.120 15 88655329 intron variant A/G snv 8.8E-02 1
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs340630
AFF1
0.925 0.120 4 87037243 intron variant G/A snv 0.42 1
rs13330176 1.000 0.120 16 85985481 upstream gene variant T/A snv 0.24 1
rs3824660
GATA3
1.000 0.120 10 8062759 intron variant C/T snv 0.49 1
rs2275806
GATA3-AS1 ; GATA3
1.000 0.120 10 8053377 non coding transcript exon variant G/A snv 0.44 1
rs998731
TPD52 ; LOC105375920
1.000 0.120 8 80183160 intron variant C/G;T snv 1
rs726288
SFTPD
1.000 0.120 10 79947217 intron variant C/T snv 2.9E-02 1
rs227163
UTS2
1.000 0.120 1 7901146 intergenic variant C/G;T snv 1
rs2867461
ANXA3
1.000 0.120 4 78592061 intron variant A/G;T snv 1
rs12901682
PSMA4
0.851 0.200 15 78540881 5 prime UTR variant A/C;T snv 1
rs954905 1.000 0.120 18 77620551 upstream gene variant A/G;T snv 1