Disease: Corpuscular Hemoglobin Concentration Mean
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
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 7
rs737092 20 57415349 regulatory region variant T/C snv 0.58 7
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 6
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 5
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 5
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 5