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
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs11672387
HOOK2 ; MAST1
19 12870439 intron variant C/G snv 0.24 3
rs73660574
GFI1B
9 132985025 intron variant G/A snv 5.3E-02 3
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs3785309
LOC107983982 ; HBM
16 162650 intron variant C/T snv 0.10 3
rs7194649
HBM ; HBZP1
16 165107 non coding transcript exon variant C/A snv 0.18 3
rs706027
BZW2
7 16660352 intron variant A/T snv 0.43 4
rs59616136
MYO9B
19 17141231 intron variant G/A snv 8.1E-02 4
rs113635136
TFRC
3 196075973 intron variant AA/-;A;AAA;AAAA delins 3
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs8067342
NATD1
17 21253548 upstream gene variant C/T snv 0.25 3
rs131656
UBE2L3
22 21563161 intron variant G/A snv 0.20 3
rs57467915
ABCB6
2 219216694 missense variant G/A snv 8.8E-03 9.6E-03 3
rs8013143
PSMB5
14 23025068 intron variant A/G snv 0.43 4
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs6803
ERAL1 ; MIR451B
17 28860771 3 prime UTR variant C/T snv 0.73 3
rs225245
AP2B1
17 35619088 intron variant A/G snv 0.39 3
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5