Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13 4
rs59616136
MYO9B
19 17141231 intron variant G/A snv 8.1E-02 4
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv 4
rs6803
ERAL1 ; MIR451B
17 28860771 3 prime UTR variant C/T snv 0.73 4
rs11735662 4 144104973 intron variant C/T snv 2.1E-02 3
rs2227930
ATR
3 142558733 synonymous variant A/T snv 0.55 0.63 3
rs6600233
NPRL3
16 93505 intron variant C/G;T snv 3
rs7853365
RCL1
9 4855858 intron variant A/C;T snv 3
rs1193
RMND5A
2 86775106 3 prime UTR variant C/T snv 0.68 2
rs1357529
PLS1 ; LOC105374136
3 142632255 intron variant T/A;C;G snv 2
rs149489081
ANK1
8 41732218 intron variant T/G snv 5.8E-03 2
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
rs4916478 3 196195699 downstream gene variant C/A;G snv 2
rs60992881
NPRL3
16 107595 intron variant AAAAAAAAA/-;A;AA;AAA;AAAA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAAAA delins 0.38 2
rs7138216 12 4225142 intergenic variant G/C snv 0.22 2
rs74417235 5 154647656 intergenic variant A/G snv 7.3E-02 2
rs7908745
MARCHF8
10 45458319 missense variant A/G snv 0.31 0.33 2
rs932223
CCDC162P
6 109265453 intron variant T/C snv 0.51 2
rs9374081
CCDC162P
6 109310579 intron variant A/G snv 0.26 2
rs9389248
HBS1L
6 134961518 3 prime UTR variant T/C snv 0.45 2
rs9914988
ERAL1 ; FAM222B
17 28856086 intron variant G/A snv 0.74 2