Disease: Body Height
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs5112
APOC1P1
1.000 0.080 19 44927023 non coding transcript exon variant C/G snv 0.55 4
rs6234
PCSK1 ; LOC101929710
0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 4
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 3
rs11599750
CPN1
10 100045685 intron variant C/T snv 0.40 2
rs12408663
NBL1 ; MICOS10-NBL1
1 19641564 intron variant T/C snv 0.19 2
rs12964
TAPBPL ; VAMP1
12 6463025 3 prime UTR variant T/C snv 0.46 2
rs182722517 19 50739310 TF binding site variant G/A snv 3.6E-03 2
rs2249350
ADAMTS5
1.000 0.080 21 26950187 intron variant C/A snv 9.7E-02 2
rs2270894
CRELD1 ; IL17RC
3 9933702 intron variant C/G snv 0.19 2
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 2