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
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs57467915
ABCB6
2 219216694 missense variant G/A snv 8.8E-03 9.6E-03 3
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs6150565
ANK1
8 41655063 3 prime UTR variant AGAGTCTATACAGC/-;AGAGTCTATACAGCAGAGTCTATACAGC delins 3
rs225245
AP2B1
17 35619088 intron variant A/G snv 0.39 3
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs706027
BZW2
7 16660352 intron variant A/T snv 0.43 4
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs3169166
DNAJA4
15 78270761 intron variant A/C snv 0.42 3
rs12050884
EIF2AK4
15 40014133 intron variant C/A snv 0.25 4
rs6803
ERAL1 ; MIR451B
17 28860771 3 prime UTR variant C/T snv 0.73 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs73660574
GFI1B
9 132985025 intron variant G/A snv 5.3E-02 3
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs7194649
HBM ; HBZP1
16 165107 non coding transcript exon variant C/A snv 0.18 3
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs11672387
HOOK2 ; MAST1
19 12870439 intron variant C/G snv 0.24 3
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
rs3785309
LOC107983982 ; HBM
16 162650 intron variant C/T snv 0.10 3
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs59616136
MYO9B
19 17141231 intron variant G/A snv 8.1E-02 4