Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs11127153
PLB1
2 28463094 intron variant T/A;C snv 2
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs11353326
ARIH2
3 48941172 intron variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA;AAAAAAA delins 2
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs11734460
PCGF3
4 711285 intron variant C/A;T snv 4
rs12545733
LOC254896
8 23099490 intron variant T/A;C snv 2
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs12968338
SERPINB13
18 63584740 upstream gene variant C/G;T snv 2
rs13056815
LIMK2
22 31272264 intron variant G/A;C snv 2
rs139707092
SPC25 ; NOSTRIN
2 168850753 intron variant TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT delins 5
rs140948517
RHBDD2
7 75857462 intron variant TT/-;T;TTT;TTTT;TTTTTTTTTTTT delins 2
rs14408
IFITM2
11 308314 missense variant T/C;G snv 0.53 4
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs147694761
NPC1
18 23571654 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 5
rs149206763
LOC105371498
17 4618946 downstream gene variant G/A;C snv 2
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs175705 14 75509305 intergenic variant C/A;G;T snv 2
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs1968252
LOC105372263
19 7782850 upstream gene variant G/A;T snv 5