Disease: Red Blood Cell Count measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs9402686
LOC105378010
6 135106679 upstream gene variant G/A snv 0.20 4
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 3
rs5756506
TMPRSS6
22 37071352 intron variant G/A;C snv 3