Disease: Red Blood Cell Count measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 7
rs3824755
CYP17A1
0.925 0.120 10 102836092 intron variant G/A;C;T snv 5
rs8069437
LRRC37A2 ; WNT3
17 46829583 intron variant T/C snv 0.82 4