Disease: Reticulocyte count (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
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
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 5
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs159058
NOL4L ; LOC101929698
20 32520305 intron variant A/C;T snv 4
rs2748424
TMC6 ; TMC8
17 78128784 intron variant C/G snv 0.26 4
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 4
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv 4
rs6592965
IKZF1
7 50360284 intron variant G/A snv 0.47 4