Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11735662 4 144104973 intron variant C/T snv 2.1E-02 3
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs4916478 3 196195699 downstream gene variant C/A;G snv 2
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs7138216 12 4225142 intergenic variant G/C snv 0.22 2
rs737092 20 57415349 regulatory region variant T/C snv 0.58 7
rs74417235 5 154647656 intergenic variant A/G snv 7.3E-02 2
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 6
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
rs2227930
ATR
3 142558733 synonymous variant A/T snv 0.55 0.63 3
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 8
rs932223
CCDC162P
6 109265453 intron variant T/C snv 0.51 2
rs9374081
CCDC162P
6 109310579 intron variant A/G snv 0.26 2
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13 4
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
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
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs9389248
HBS1L
6 134961518 3 prime UTR variant T/C snv 0.45 2
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs3817621
KLF1
19 12887391 upstream gene variant G/C;T snv 0.25 2
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6