Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs129129
TRIM38
0.925 0.120 6 25960801 upstream gene variant A/G snv 0.73 5
rs13197601
SLC17A1
0.882 0.200 6 25785707 intron variant G/A snv 0.32 5
rs150551
CARMIL1
0.925 0.120 6 25533702 intron variant A/G;T snv 4
rs1540275 0.925 0.120 6 26036248 upstream gene variant T/A;C snv 4
rs1540276
H4C2
0.925 0.120 6 26028591 upstream gene variant T/A;G snv 5
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs198853
H4C3
0.925 0.120 6 26103868 upstream gene variant T/C snv 0.28 5
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199736 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs199739 0.925 0.120 6 25960281 upstream gene variant A/C;G snv 0.78 5
rs199750 0.882 0.160 6 26016234 upstream gene variant C/T snv 0.77 5
rs199751 0.925 0.120 6 26015355 upstream gene variant T/C snv 0.77 5
rs199752 0.925 0.120 6 26012647 upstream gene variant C/T snv 0.77 5
rs199753 0.925 0.120 6 26001660 non coding transcript exon variant G/A snv 0.77 5
rs1997672
CARMIL1
0.925 0.120 6 25617316 intron variant T/G snv 0.28 4
rs2032447
H3C3 ; H2BC3 ; H2AC5P
0.925 0.120 6 26044141 non coding transcript exon variant A/G snv 4.1E-06; 0.67 0.67 6
rs2051541 0.925 0.120 6 25944983 regulatory region variant A/G snv 0.47 4
rs2077393
CARMIL1
6 25607137 intron variant C/T snv 0.29 2
rs2213284
H3C2
0.925 0.120 6 26031640 3 prime UTR variant G/A snv 0.70 0.76 4
rs2230655
H2AC4 ; H3C2
0.882 0.160 6 26033278 synonymous variant G/A snv 0.71 0.76 5
rs2762353
SLC17A1
0.882 0.200 6 25794203 intron variant A/G snv 0.66 5
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs3757131
SLC17A1
0.882 0.200 6 25783681 intron variant C/T snv 0.32 5