Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13 4
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs11735662 4 144104973 intron variant C/T snv 2.1E-02 3
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs1193
RMND5A
2 86775106 3 prime UTR variant C/T snv 0.68 2
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 5
rs1357529
PLS1 ; LOC105374136
3 142632255 intron variant T/A;C;G snv 2
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs149489081
ANK1
8 41732218 intron variant T/G snv 5.8E-03 2
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 7
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs2227930
ATR
3 142558733 synonymous variant A/T snv 0.55 0.63 3
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 5
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs3817621
KLF1
19 12887391 upstream gene variant G/C;T snv 0.25 2
rs3896594
LOC105373411
2 8622284 intron variant T/G snv 0.50 2
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
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
rs59616136
MYO9B
19 17141231 intron variant G/A snv 8.1E-02 4