Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs10138752
RAD51B
14 68713254 intron variant C/T snv 8.8E-02 5
rs10165200
LINC00299
2 8299499 intron variant G/A snv 0.36 2
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs10265538 7 20502242 intergenic variant T/C snv 0.20 2
rs10283564
INSL6 ; JAK2
9 5075628 intron variant C/G snv 0.23 2
rs1032726
CD200R1
3 112967228 intron variant T/C snv 0.46 2
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70 2
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs10410864 19 39711776 downstream gene variant T/C snv 0.68 2
rs10542411 2 61541105 upstream gene variant ATATT/-;ATATTATATT delins 0.23 2
rs1057258
INPP5D
2 233206983 3 prime UTR variant C/T snv 0.30 3
rs10852622
ZFPM1
16 88490472 intron variant A/G snv 0.35 2
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs10893844 11 128315955 regulatory region variant G/C snv 0.36 2
rs10995240
LOC105378327 ; ZNF365
10 62628871 intron variant G/C snv 0.29 2
rs11127153
PLB1
2 28463094 intron variant T/A;C snv 2
rs111759324 1 101186966 upstream gene variant C/T snv 0.11 2
rs111930700
ACVR1B
12 51967869 intron variant C/G snv 8.4E-02 4
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs11319879
HHEX
10 92693719 intron variant A/- delins 0.53 2
rs11327184
CCDC26
8 129592027 intron variant C/- delins 0.40 4
rs113422568
SUFU
10 102578181 intron variant G/A snv 0.25 2
rs11353326
ARIH2
3 48941172 intron variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA;AAAAAAA delins 2