Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs1178979
BAZ1B
0.925 0.120 7 73442100 3 prime UTR variant T/C snv 0.21 6
rs11974409
TBL2
0.925 0.120 7 73575060 intron variant A/G snv 0.16 6
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs13232120
TBL2
0.925 0.120 7 73568980 3 prime UTR variant A/T snv 0.11 6
rs17145713
BAZ1B
0.925 0.120 7 73490480 intron variant C/T snv 0.21 6
rs1919127
C2orf16
0.925 0.120 2 27578626 missense variant T/C snv 0.31 0.27 6
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs10208529
C2orf16
0.925 0.120 2 27563321 intron variant A/T snv 0.28 5
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs1178977
BAZ1B
0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21 5
rs11983997 0.925 0.120 7 73524914 upstream gene variant G/A;C snv 5
rs12467476
ZNF512
0.925 0.120 2 27602848 intron variant T/C snv 0.23 5
rs12478841
ZNF512
0.925 0.120 2 27588855 intron variant A/G snv 0.27 5
rs12539316 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 5
rs129129
TRIM38
0.925 0.120 6 25960801 upstream gene variant A/G snv 0.73 5
rs13002853
CCDC121 ; GPN1
0.925 0.120 2 27630378 intron variant C/G snv 0.20 5