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
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 7
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs7766720
LINC02532
6 106725104 non coding transcript exon variant T/C snv 0.16 3
rs10767873
LOC101928338
11 30747131 intergenic variant C/T snv 0.35 2