Disease: Finding of Mean Corpuscular Hemoglobin
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
rs113525195
PSMB5
14 23030112 intron variant C/A;T snv 2
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs11771301
WIPI2
7 5195031 intron variant C/G;T snv 2
rs140446749
SPTA1
1 158668470 intron variant G/A snv 8.0E-03 2
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs159058
NOL4L ; LOC101929698
20 32520305 intron variant A/C;T snv 4
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
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
rs4832312
RMND5A
2 86762839 intron variant G/A;C snv 3
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv 4
rs6592965
IKZF1
7 50360284 intron variant G/A snv 0.47 4
rs6600233
NPRL3
16 93505 intron variant C/G;T snv 2
rs706027
BZW2
7 16660352 intron variant A/T snv 0.43 4
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
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs35259020 9 134085798 intergenic variant CT/- delins 0.18 3
rs35788208 5 154654616 intergenic variant C/T snv 7.4E-02 2
rs875741 5 173860848 intergenic variant G/A;C snv 3