Disease: Red cell distribution width determination
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11021221 11 95575690 intron variant T/A;G snv 4
rs113635136
TFRC
3 196075973 intron variant AA/-;A;AAA;AAAA delins 3
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs6150565
ANK1
8 41655063 3 prime UTR variant AGAGTCTATACAGC/-;AGAGTCTATACAGCAGAGTCTATACAGC delins 3
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs57467915
ABCB6
2 219216694 missense variant G/A snv 8.8E-03 9.6E-03 3
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs73660574
GFI1B
9 132985025 intron variant G/A snv 5.3E-02 3
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs59616136
MYO9B
19 17141231 intron variant G/A snv 8.1E-02 4
rs3785309
LOC107983982 ; HBM
16 162650 intron variant C/T snv 0.10 3
rs74035509
ZFPM1
16 88500925 intron variant C/T snv 0.10 5
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs7194649
HBM ; HBZP1
16 165107 non coding transcript exon variant C/A snv 0.18 3
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs131656
UBE2L3
22 21563161 intron variant G/A snv 0.20 3
rs11672387
HOOK2 ; MAST1
19 12870439 intron variant C/G snv 0.24 3
rs8067342
NATD1
17 21253548 upstream gene variant C/T snv 0.25 3
rs12050884
EIF2AK4
15 40014133 intron variant C/A snv 0.25 4
rs2748425
TMC8 ; TMC6
17 78128765 5 prime UTR variant G/C snv 0.26 3
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5