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
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs3809627
TBX6 ; YPEL3
16 30091839 5 prime UTR variant C/A snv 0.41 5
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs78744187 19 33263642 intergenic variant C/T snv 6.8E-02 5