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
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 17
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 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
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6
rs4791641
PFAS
17 8257831 missense variant C/T snv 0.43 0.41 4
rs17561950
PGS1
17 78396063 intron variant G/A snv 0.45 3