Disease: Body Height
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 4
rs10482795
TGFB2
1 218432267 intron variant G/A;T snv 2
rs12330322
RYBP
3 72406204 intron variant C/A;T snv 2
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs3764419
ATAD5
17 30837005 intron variant C/A;G snv 3
rs4800452
CABLES1
18 23147647 intron variant C/G;T snv 3
rs4842838
ADAMTSL3
15 83913372 missense variant G/A;T snv 1.6E-05; 0.61 3
rs4868126 5 171856465 regulatory region variant T/A;G snv 2
rs6684205
TGFB2
1 218436360 intron variant A/G;T snv 3
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs757608 17 61419916 regulatory region variant A/G;T snv 4
rs975210
TLE3
15 70072013 intron variant G/A snv 0.16 2
rs3817428
ACAN
15 88872016 missense variant C/G snv 0.20 0.20 3
rs798489
GNA12 ; AMZ1
7 2762169 splice donor variant C/T snv 0.20 4
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs3791675
EFEMP1
1.000 0.040 2 55884174 intron variant C/T snv 0.20 4
rs11694842
DNMT3A
2 25260101 intron variant A/G snv 0.22 2
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs10946808
H2AC9P
1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26 5
rs4886782
LOXL1
1.000 0.040 15 73936469 intron variant G/A snv 0.27 5
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 5
rs1926872 1 184049341 upstream gene variant T/C snv 0.29 2