Disease: Body Height
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1064939
TTC36 ; LOC101929089 ; KMT2A
11 118525616 3 prime UTR variant A/T snv 1.4E-02 2
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs12449442
BPTF
17 67951524 non coding transcript exon variant G/A snv 0.22 3
rs12939056
KDM6B ; LOC107987244
17 7851675 synonymous variant G/A;C snv 0.38; 2.2E-04 2
rs12967135 18 60181790 intergenic variant G/A snv 0.24 7
rs145878042
RAPGEF3
12 47749532 missense variant A/G snv 7.3E-03 7.6E-03 3
rs1541777
TTLL4
2 218722568 intron variant A/G snv 0.51 2
rs1582931 5 123321505 intergenic variant G/A;T snv 2
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2145270 20 6641038 regulatory region variant C/T snv 0.61 3
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs34720381
PRRC2C
1 171486183 intron variant C/T snv 7.3E-02 4
rs6422513
EVI5
1 92566910 intron variant G/A;C snv 2
rs6823268
ANAPC10
4 145061411 intron variant A/G snv 0.28 2
rs7534091 1 118321993 intergenic variant A/G snv 0.23 2
rs76929617 12 120429995 intergenic variant A/G snv 3.7E-02 2
rs7826312
NRG1
8 32542597 intron variant T/C snv 0.57 2
rs9880211
STAG1
3 136388707 intron variant G/A snv 0.19 2
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 8
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 5
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6