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
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs11021221 11 95575690 intron variant T/A;G snv 4
rs113635136
TFRC
3 196075973 intron variant AA/-;A;AAA;AAAA delins 3
rs11672387
HOOK2 ; MAST1
19 12870439 intron variant C/G snv 0.24 3
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs12050884
EIF2AK4
15 40014133 intron variant C/A snv 0.25 4
rs131656
UBE2L3
22 21563161 intron variant G/A snv 0.20 3
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs225245
AP2B1
17 35619088 intron variant A/G snv 0.39 3
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 4
rs3169166
DNAJA4
15 78270761 intron variant A/C snv 0.42 3
rs3785309
LOC107983982 ; HBM
16 162650 intron variant C/T snv 0.10 3
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs59616136
MYO9B
19 17141231 intron variant G/A snv 8.1E-02 4
rs706027
BZW2
7 16660352 intron variant A/T snv 0.43 4
rs73660574
GFI1B
9 132985025 intron variant G/A snv 5.3E-02 3
rs74035509
ZFPM1
16 88500925 intron variant C/T snv 0.10 5
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
rs8013143
PSMB5
14 23025068 intron variant A/G snv 0.43 4
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55