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
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6