Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3917914
CSF3R
1 36482287 intron variant G/A;T snv 5
rs397731840
CCDC26
8 129599504 intron variant TT/-;T;TTT;TTTT;TTTTT delins 5
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs6500550
TRAP1
16 3696240 intron variant C/G;T snv 5
rs66505542
BUD13
11 116752498 intron variant AA/-;A;AAA delins 5
rs8179
CDK6
0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 5
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv 5
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 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
rs2239630
CEBPE
0.925 0.160 14 23120140 upstream gene variant A/C;G snv 4
rs301807
RERE-AS1 ; RERE
0.925 0.080 1 8424763 intron variant A/G;T snv 4
rs34293785 1 65671509 intergenic variant T/C snv 4
rs398032702
C18orf25
18 46245574 intron variant AA/-;A;AAA;AAAA;AAAAAAA;AAAAAAAAAAAAA delins 4
rs45577137
CEBPD
8 47739071 upstream gene variant A/G;T snv 4
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 4
rs575404063 19 18405498 intergenic variant AAA/-;A;AA;AAAA;AAAAA delins 4
rs71191701 9 136427805 downstream gene variant G/C;T snv 4
rs7288670
GGT5
22 24225858 intron variant A/C;G snv 4
rs77697917 17 43763481 upstream gene variant C/G;T snv 4