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
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 8
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 5
rs9292468 5 32818967 intergenic variant T/A;C snv 5
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 4
rs1173727 5 32830415 intergenic variant T/C snv 0.66 3
rs1239948
DLEU1 ; DLEU7
13 50532386 intron variant A/T snv 0.59 3
rs42377
CDK6
7 92614358 3 prime UTR variant G/A snv 0.28 3
rs592373
LSP1
0.925 0.080 11 1869760 intron variant G/A;T snv 0.63; 6.8E-06 3
rs1036821
ZFAT
8 134638240 intron variant G/A snv 0.28 2
rs17010957
ARHGAP24
4 85798012 intron variant T/A;C snv 2
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 2
rs2196792
DNAJC27-AS1
2 25037084 non coding transcript exon variant A/G snv 0.73 2
rs2289125
NOX4
11 89491285 5 prime UTR variant A/C snv 0.69 0.61 2