Disease: Body Height
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 9
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs7689420
HHIP-AS1 ; HHIP
0.851 0.080 4 144647200 non coding transcript exon variant T/C snv 0.79 7
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 7
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
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 6
rs10946808
H2AC9P
1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26 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
rs4896582
ADGRG6
6 142382740 intron variant G/A snv 0.50 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
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 4
rs1330
NUCB2
1.000 0.080 11 17294482 intron variant C/T snv 0.30 4
rs3791675
EFEMP1
1.000 0.040 2 55884174 intron variant C/T snv 0.20 4
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 4
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs757608 17 61419916 regulatory region variant A/G;T snv 4
rs798489
GNA12 ; AMZ1
7 2762169 splice donor variant C/T snv 0.20 4