Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10090114
MSRA
8 10147444 intron variant T/C snv 0.90 1
rs1018827
F5
1 169544768 intron variant A/G snv 0.92 1
rs1021230
EBF2
8 25928927 intron variant A/T snv 0.27 1
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs1048483
SMG6 ; HIC1
17 2063163 3 prime UTR variant C/T snv 0.43 1
rs10498632
TC2N
14 91824400 intron variant A/G snv 0.29 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs10746487 1 9278630 intergenic variant T/A;C snv 1
rs10747514
PROCR ; MMP24-AS1-EDEM2
20 35187566 intron variant G/A snv 0.40 1
rs10886430
GRK5
10 119250744 intron variant A/G snv 8.8E-02 3
rs10919507 1 170885468 intron variant C/T snv 3.0E-02 1
rs11057270
SBNO1
12 123323526 intron variant T/C snv 0.28 1
rs11158204
LOC105370522
14 58377808 intron variant C/T snv 0.25 1
rs113092656 0.882 0.120 6 11615072 intergenic variant G/A snv 2.6E-02 5
rs113451833 8 64970119 downstream gene variant G/T snv 0.18 1
rs113976843
LINC01681
1 170254627 intron variant T/C snv 8.6E-03 1
rs114149445
F2RL2 ; IQGAP2
5 76625137 intron variant C/T snv 4.7E-03 1
rs114209171
FUNDC2
0.882 0.120 X 155050522 non coding transcript exon variant T/C snv 0.23 5
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 1
rs115063924 1 168741790 intron variant C/A;T snv 6.7E-03 1
rs115405361
LOC105375959 ; LINC01231
9 3193201 intron variant T/C snv 1.9E-02 1
rs115865014
TBC1D5 ; SATB1
3 18424258 5 prime UTR variant A/C snv 1.2E-02 1
rs117390891
LOC100505664
20 23187889 intron variant G/T snv 0.13 1
rs117784795
PTPRJ
11 48030514 intron variant C/T snv 1.2E-02 1
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 1