Disease: White Blood Cell Count procedure
Source: ALL
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
rs10206089 2 61476184 intron variant G/A snv 4
rs10995477
JMJD1C
10 63250912 intron variant T/C snv 0.43 4
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs11624512
RIN3
14 92644775 non coding transcript exon variant C/T snv 0.15 5
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs12101888
EHD4
15 41939155 intron variant C/T snv 0.34 3
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs12450688
PSMD3
17 39987976 intron variant G/A snv 0.56 3
rs12542907 8 67900953 intergenic variant C/G snv 0.29 5
rs12550612
TNFRSF10C
8 23109256 intron variant G/A snv 0.83 5
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs13033745
MEIS1 ; MEIS1-AS3
2 66433271 intron variant G/T snv 0.67 2
rs13138355 4 82624823 upstream gene variant C/A;T snv 4
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs139707092
SPC25 ; NOSTRIN
2 168850753 intron variant TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT delins 5
rs143699489 3 141208279 intergenic variant A/G snv 0.22 4
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 5