Disease: Reticulocyte count (procedure)
Source: ALL
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 92
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs11735662 4 144104973 intron variant C/T snv 2.1E-02 3
rs10828725
PRTFDC1
10 24929314 intron variant G/T snv 0.26 2
rs4728335 7 134697578 regulatory region variant G/C snv 0.33 2
rs79047930
PTPRN
2 219300805 intron variant C/T snv 1.8E-02 2