Disease: Reticulocyte count (procedure)
Source: GWASCAT ×
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 61
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs2968478 16 88792238 intergenic variant T/G snv 0.61 4
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 3
rs567292015
LOC100289580 ; PIEZO1
16 88732112 intron variant G/- delins 4.6E-03 2