Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1870293
SETD1A
0.827 0.120 16 30959620 intron variant T/C snv 0.62 6
rs10782001
FBXL19
1.000 0.040 16 30931304 intron variant G/A snv 0.53 2
rs13708
STX1B ; HSD3B7
1.000 0.040 16 30989488 3 prime UTR variant G/A;C snv 0.52 2
rs887466
POU5F1 ; PSORS1C3
1.000 0.040 6 31175734 intron variant G/A snv 0.40 2