Disease: White Blood Cell Count procedure
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 14
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs61754230
RAB21
12 71785666 missense variant C/T snv 1.3E-02 1.2E-02 4
rs11264483
C1orf61
1 156436589 intron variant G/C snv 0.45 2
rs9904177
MINK1
17 4852129 intron variant A/G snv 0.32 2