Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs60992881
NPRL3
16 107595 intron variant AAAAAAAAA/-;A;AA;AAA;AAAA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAAAA delins 0.38 2
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv 4
rs6600233
NPRL3
16 93505 intron variant C/G;T snv 3
rs6803
ERAL1 ; MIR451B
17 28860771 3 prime UTR variant C/T snv 0.73 4
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
rs7853365
RCL1
9 4855858 intron variant A/C;T snv 3
rs7908745
MARCHF8
10 45458319 missense variant A/G snv 0.31 0.33 2
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 6
rs932223
CCDC162P
6 109265453 intron variant T/C snv 0.51 2
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
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
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs9914988
ERAL1 ; FAM222B
17 28856086 intron variant G/A snv 0.74 2
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 5
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 8
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226