Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3791675
rs3791675
2 55884174 intron variant C/T snp 0.22
CUI: C0005890
Disease: Body Height
Body Height
0.800 5 2008 2015
dbSNP: rs1042725
rs1042725
12 65964567 3 prime UTR variant C/T snp 0.48
CUI: C0005890
Disease: Body Height
Body Height
0.800 4 2007 2015
dbSNP: rs10748128
rs10748128
12 69433878 intergenic variant G/T snp 0.42
CUI: C0005890
Disease: Body Height
Body Height
0.800 4 2010 2015
dbSNP: rs2093210
rs2093210
14 60490561 intron variant C/T snp 0.47
CUI: C0005890
Disease: Body Height
Body Height
0.800 4 2010 2015
dbSNP: rs2284746
rs2284746
1 16980180 intron variant C/A,G snp 3.2E-05; 0.41
CUI: C0005890
Disease: Body Height
Body Height
0.800 4 2010 2015
dbSNP: rs3791679
rs3791679
2 55869757 intron variant A/G snp 0.22
CUI: C0005890
Disease: Body Height
Body Height
0.800 4 2008 2014
dbSNP: rs7466269
rs7466269
9 130588697 intron variant A/G snp 0.34
CUI: C0005890
Disease: Body Height
Body Height
0.800 4 2008 2014
dbSNP: rs806794
rs806794
6 26200449 3 prime UTR variant A/G snp 0.37
CUI: C0005890
Disease: Body Height
Body Height
0.800 4 2010 2015
dbSNP: rs8756
rs8756
12 65965972 3 prime UTR variant C/A snp 0.55
CUI: C0005890
Disease: Body Height
Body Height
0.800 4 2008 2014
dbSNP: rs10946808
rs10946808
1.000 0.036 6 26233159 non coding transcript exon variant A/G snp 0.28
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2009
dbSNP: rs10958476
rs10958476
8 56183249 intron variant T/C snp 0.17
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2014
dbSNP: rs11107116
rs11107116
12 93584728 intergenic variant G/A,T snp 3.2E-05; 0.20
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2015
dbSNP: rs11144688
rs11144688
9 75927370 intron variant G/A snp 9.3E-02
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2010 2014
dbSNP: rs11205277
rs11205277
1 149920979 intergenic variant A/C,G,T snp 3.2E-05; 0.31; 9.6E-05
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2015
dbSNP: rs1490384
rs1490384
6 126530014 intergenic variant C/G,T snp 0.44
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2010 2017
dbSNP: rs1776897
rs1776897
6 34227234 regulatory region variant G/T snp 0.81
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2015
dbSNP: rs1812175
rs1812175
4 144653692 intron variant A/G snp 0.79
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2014
dbSNP: rs1950500
rs1950500
14 24361644 intergenic variant T/C snp 0.69
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2010 2014
dbSNP: rs2079795
rs2079795
17 61419288 intergenic variant T/A,C snp 0.62
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2010 2014
dbSNP: rs2280470
rs2280470
15 88852395 intron variant A/G snp 0.67
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2010 2014
dbSNP: rs2282978
rs2282978
7 92635096 intron variant T/C snp 0.37
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2009
dbSNP: rs2856321
rs2856321
12 11702839 intron variant G/A snp 0.51
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2010 2014
dbSNP: rs526896
rs526896
5 135021015 intergenic variant T/A,G snp 0.27
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2010 2015
dbSNP: rs572169
rs572169
1.000 0.071 3 172447937 synonymous variant C/T snp 0.31 0.25
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2010 2015
dbSNP: rs6060369
rs6060369
20 35319358 intron variant T/C snp 0.48
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2015