Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11405616
NDFIP1
5 142130697 intron variant A/-;AA;AAA;AAAA delins 4
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs11734460
PCGF3
4 711285 intron variant C/A;T snv 4
rs14408
IFITM2
11 308314 missense variant T/C;G snv 0.53 4
rs146318841
AHI1
6 135328483 intron variant TGCCATAAACCATAGCCATAG/-;TGCCATAAACCATAGCCATAGTGCCATAAACCATAGCCATAG delins 4
rs398032702
C18orf25
18 46245574 intron variant AA/-;A;AAA;AAAA;AAAAAAA;AAAAAAAAAAAAA delins 4
rs575404063 19 18405498 intergenic variant AAA/-;A;AA;AAAA;AAAAA delins 4
rs71191701 9 136427805 downstream gene variant G/C;T snv 4
rs778387 1 56158423 intron variant C/A;G;T snv 4
rs791357
LOC107986482
5 173778222 downstream gene variant T/A;C snv 4
rs11741826
CCDC125
5 69294573 intron variant G/A;C snv 3
rs1969949
DOCK8
9 305428 intron variant T/A;C;G snv 3
rs28476539
SCD5
4 82631138 3 prime UTR variant G/A;T snv 3
rs5820258
ARHGAP23
17 38437623 intron variant CC/-;C;CCC;CCCC;CCCCC delins 3
rs8068017 17 1417822 downstream gene variant T/A;C snv 3
rs5747327
BCL2L13
22 17686446 intron variant T/A;C;G snv 1
rs930232
CNN2
19 1036019 intron variant G/A;C snv 0.44 1
rs9872440
ACKR2 ; KRBOX1
3 42854959 intron variant T/C;G snv 1
rs555346412
HECTD4
12 112191863 intron variant G/C snv 8.2E-04 5
rs55799208
CXCR2
2 218135259 missense variant G/A snv 1.4E-03 1.4E-03 5
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs138488218 12 53354069 regulatory region variant A/T snv 7.6E-03 4
rs146890554
CSF3
17 40017384 3 prime UTR variant C/T snv 9.6E-03 5