Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 3
rs10158467 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 2
rs10187276 0.925 0.080 2 227805721 upstream gene variant T/C snv 0.62 2
rs10836538
PRR5L
0.925 0.080 11 36343703 intron variant G/T snv 0.30 2
rs1117490
TRIM26
0.925 0.080 6 30202733 intron variant T/C snv 0.24 2
rs11178648
TSPAN8
0.925 0.080 12 71139430 intron variant C/T snv 0.29 2
rs111863753
GBA3
1.000 0.080 4 22794376 intron variant G/A snv 7.4E-03 2
rs113010607
SEPTIN8
0.925 0.080 5 132770006 intron variant T/C snv 0.21 2
rs113092121
KIF11
0.925 0.080 10 92624756 intron variant -/CTCT delins 2
rs11412402
EEFSEC
0.925 0.080 3 128194003 intron variant -/T ins 0.65 2
rs114444221
HLA-B
0.925 0.080 6 31335547 intron variant A/G snv 0.18 2
rs117097909
GSDMB
0.925 0.080 17 39908718 intron variant G/A snv 4.7E-02 2
rs117420762
SLC2A10
1.000 0.080 20 46719767 intron variant C/A snv 5.8E-03 2
rs12023876
ADORA1
0.925 0.080 1 203124073 intron variant G/A;T snv 2
rs12531500 0.925 0.080 7 20504586 intergenic variant A/C;G snv 2
rs12935657
CLEC16A
0.925 0.080 16 11125184 intron variant G/A snv 0.18 2
rs12964116
SERPINB7
0.925 0.080 18 63775385 5 prime UTR variant A/G snv 3.0E-02 2
rs12965763
POLI
0.925 0.080 18 54290038 intron variant G/A snv 0.18 2
rs13090972 1.000 0.080 3 89027746 intergenic variant C/G;T snv 2
rs1321859
LOC105377891
0.925 0.080 6 90301954 intron variant C/T snv 0.24 2
rs13416555
LINC00299
1.000 0.080 2 8301605 intron variant C/A;G snv 2
rs137939366
ELSPBP1
1.000 0.080 19 48019433 intron variant T/- del 1.5E-02 2
rs140179402
BCL2L13
1.000 0.080 22 17685512 intron variant C/T snv 1.2E-02 2
rs140522418
LOC107984408
0.925 0.080 11 128302942 intergenic variant A/-;AA delins 2
rs142161979
ANKS1B
1.000 0.080 12 99392036 intron variant G/C snv 3.5E-03 2