Disease: Body Height
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2145270 20 6641038 regulatory region variant C/T snv 0.61 3
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs12449442
BPTF
17 67951524 non coding transcript exon variant G/A snv 0.22 3
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs12939056
KDM6B ; LOC107987244
17 7851675 synonymous variant G/A;C snv 0.38; 2.2E-04 2
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs6422513
EVI5
1 92566910 intron variant G/A;C snv 2
rs6234
PCSK1 ; LOC101929710
0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 4