Disease: RDW - Red blood cell distribution width result
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
rs8013143
PSMB5
14 23025068 intron variant A/G snv 0.43 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
rs131656
UBE2L3
22 21563161 intron variant G/A snv 0.20 3
rs225245
AP2B1
17 35619088 intron variant A/G snv 0.39 3
rs2748425
TMC8 ; TMC6
17 78128765 5 prime UTR variant G/C snv 0.26 3
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
rs57467915
ABCB6
2 219216694 missense variant G/A snv 8.8E-03 9.6E-03 3
rs6150565
ANK1
8 41655063 3 prime UTR variant AGAGTCTATACAGC/-;AGAGTCTATACAGCAGAGTCTATACAGC delins 3
rs6803
ERAL1 ; MIR451B
17 28860771 3 prime UTR variant C/T snv 0.73 3
rs7194649
HBM ; HBZP1
16 165107 non coding transcript exon variant C/A snv 0.18 3
rs73660574
GFI1B
9 132985025 intron variant G/A snv 5.3E-02 3
rs8067342
NATD1
17 21253548 upstream gene variant C/T snv 0.25 3