Disease: Body Height
Source: ALL
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 92
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs110419
LOC105376536 ; LMO1
0.827 0.200 11 8231306 intron variant A/G snv 0.42 8
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs9292468 5 32818967 intergenic variant T/A;C snv 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 5
rs592373
LSP1
0.925 0.080 11 1869760 intron variant G/A;T snv 0.63; 6.8E-06 5
rs1126464
DPEP1
1.000 0.040 16 89637957 missense variant G/A;C snv 1.3E-05; 0.26 4
rs117870289
ERG
21 38611524 intron variant C/T snv 7.7E-03 2
rs11899888
EFEMP1
2 55875609 intron variant A/G snv 0.11 2
rs17880989
MMP14
14 22844424 missense variant G/A snv 1.6E-02 1.5E-02 2
rs36226649
NFATC4
14 24366294 intron variant T/C snv 4.1E-02 2
rs4709746
LOC105378105 ; LOC107986666
6 163711969 intron variant C/T snv 0.10 2
rs7980687
SBNO1
12 123338164 intron variant G/A snv 0.22 2