Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs55799208
CXCR2
2 218135259 missense variant G/A snv 1.4E-03 1.4E-03 5
rs78487399
THADA
2 43582208 intron variant G/C snv 6.2E-02 5
rs9287604 2 236867522 intergenic variant G/C snv 0.62 5
rs10206089 2 61476184 intron variant G/A snv 4
rs2029582
IL1RN
2 113106194 upstream gene variant T/C snv 0.56 4
rs200476039
EML6
2 54760823 intron variant TTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT delins 5.5E-02 3
rs7575217
TBC1D8
2 101160470 intron variant A/G snv 0.68 3
rs2860773
LOC105374780
2 65438507 intron variant G/T snv 0.41 1
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs9819371
RASA2
3 141487958 intron variant C/T snv 4.7E-02 5
rs143699489 3 141208279 intergenic variant A/G snv 0.22 4
rs11920354
KIF9-AS1
3 47220756 intron variant C/A snv 0.34 3
rs2734031 3 128582547 intergenic variant T/C snv 0.90 1
rs9872440
ACKR2 ; KRBOX1
3 42854959 intron variant T/C;G snv 1
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs11734460
PCGF3
4 711285 intron variant C/A;T snv 4
rs11931598
LOC100129931 ; TADA2B
4 7045375 intron variant C/T snv 0.55 4
rs1352846
GC
4 71752058 intron variant A/G snv 0.22 4
rs58548501 4 54635119 intergenic variant -/A;ATTTTTTTTTA ins 0.43 4
rs28476539
SCD5
4 82631138 3 prime UTR variant G/A;T snv 3
rs62312418
CXCL6
4 73835795 upstream gene variant G/A snv 0.34 3
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12