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
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs9914988
ERAL1 ; FAM222B
17 28856086 intron variant G/A snv 0.74 2
rs6803
ERAL1 ; MIR451B
17 28860771 3 prime UTR variant C/T snv 0.73 4
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs149489081
ANK1
8 41732218 intron variant T/G snv 5.8E-03 2
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13 4
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs7138216 12 4225142 intergenic variant G/C snv 0.22 2
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 5
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs7908745
MARCHF8
10 45458319 missense variant A/G snv 0.31 0.33 2
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 5
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs7853365
RCL1
9 4855858 intron variant A/C;T snv 3
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
rs737092 20 57415349 regulatory region variant T/C snv 0.58 7
rs3896594
LOC105373411
2 8622284 intron variant T/G snv 0.50 2
rs1193
RMND5A
2 86775106 3 prime UTR variant C/T snv 0.68 2
rs6600233
NPRL3
16 93505 intron variant C/G;T snv 3
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6