Disease: Red Blood Cell Count measurement
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
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs12315434
R3HDM2
1.000 0.040 12 57387153 intron variant A/C snv 0.16 2