Disease: Red cell distribution width determination
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 13
rs12777
MIR3936HG ; SLC22A4
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 6