Source: GWASDB

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 4 2008 2015
dbSNP: rs6440003
rs6440003
3 141375367 intron variant G/A snp 0.53
CUI: C0005890
Disease: Body Height
Body Height
0.800 4 2008 2011
dbSNP: rs1042725
rs1042725
12 65964567 3 prime UTR variant C/T snp 0.48
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2007 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: 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: rs2282978
rs2282978
7 92635096 intron variant T/C snp 0.37
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2009
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 3 2010 2015
dbSNP: rs3791679
rs3791679
2 55869757 intron variant A/G snp 0.22
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2014
dbSNP: rs7466269
rs7466269
9 130588697 intron variant A/G snp 0.34
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2014
dbSNP: rs8756
rs8756
12 65965972 3 prime UTR variant C/A snp 0.55
CUI: C0005890
Disease: Body Height
Body Height
0.800 3 2008 2014
dbSNP: rs10472828
rs10472828
5 32888712 intergenic variant C/T snp 0.40
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2009 2009
dbSNP: rs10513137
rs10513137
3 141424588 intron variant G/A,C snp 0.16
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2009 2010
dbSNP: rs10748128
rs10748128
12 69433878 intergenic variant G/T snp 0.42
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2010 2015
dbSNP: rs10906982
rs10906982
15 83899406 intron variant T/A snp 0.61
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2008 2010
dbSNP: rs10958476
rs10958476
8 56183249 intron variant T/C snp 0.17
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 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 2 2008 2015
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 2 2008 2015
dbSNP: rs1150781
rs1150781
6 34246545 missense variant C/A,G snp 9.0E-06; 0.85 0.81
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2011 2011
dbSNP: rs11658329
rs11658329
17 63685671 intron variant G/C snp 0.38
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2011 2012
dbSNP: rs12393627
rs12393627
X 2967682 intron variant A/G snp 0.10
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2011 2012
dbSNP: rs1351394
rs1351394
12 65958046 3 prime UTR variant T/C,G snp 0.55
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2010 2013
dbSNP: rs1490384
rs1490384
6 126530014 intergenic variant C/G,T snp 0.44
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2010 2017
dbSNP: rs16942341
rs16942341
15 88845674 synonymous variant C/T snp 3.8E-02 5.3E-02
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2010 2011
dbSNP: rs17511102
rs17511102
2 37733470 A/G,T snp 5.2E-03; 5.3E-02
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2010 2013
dbSNP: rs1787200
rs1787200
DYM
18 49061284 intron variant G/A snp 0.71
CUI: C0005890
Disease: Body Height
Body Height
0.800 2 2011 2012