Disease: Body Height
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 6
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 5
rs4886782
LOXL1
1.000 0.040 15 73936469 intron variant G/A snv 0.27 5
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs1776897 6 34227234 regulatory region variant G/T snv 0.80 4
rs2638953
CCDC91
12 28381482 intron variant G/C;T snv 4
rs3760318
ADAP2
17 30920697 intron variant G/A snv 0.39 4
rs473902
PTCH1
9 95493953 intron variant T/G snv 5.7E-02 4
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs7697556 4 72649596 intergenic variant T/A;C snv 4
rs822531 7 148932667 intergenic variant C/T snv 0.85 3
rs1150668
ZNF192P1
6 28162011 intron variant T/G snv 0.58 2