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: rs2284746
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 3 2010 2013
dbSNP: rs10512248
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2008 2011
dbSNP: rs10513137
rs10513137
ZBTB38
3 141424588 intron variant G/A;C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2009 2010
dbSNP: rs11107116
rs11107116
SOCS2
1.000 0.080 12 93584728 downstream gene variant G/A;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2008 2010
dbSNP: rs11205277
rs11205277 		1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2008 2010
dbSNP: rs1150781
rs1150781
HMGA1 ; SMIM29
6 34246545 missense variant C/A;G snv 9.0E-06; 0.85
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2011 2011
dbSNP: rs1351394
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs1490384
rs1490384 		6 126530014 intron variant C/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs17511102
rs17511102
CDC42EP3 ; LOC105374465
2 37733470 intron variant A/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs2079795
rs2079795 		17 61419288 regulatory region variant T/A;C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs3764419
rs3764419
ATAD5
17 30837005 intron variant C/A;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs4842838
rs4842838
ADAMTSL3
15 83913372 missense variant G/A;T snv 1.6E-05; 0.61
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2009 2010
dbSNP: rs526896
rs526896
LOC107986452
5 135021015 intergenic variant T/A;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs9967417
rs9967417
DYM
18 49433130 intron variant G/C;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs10010325
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs10037512
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs1029534
rs1029534
JAZF1
7 28149464 intron variant T/C;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs1046934
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs10874746
rs10874746
DIPK1A
1 92858414 intron variant T/A;C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs11024739
rs11024739
SPTY2D1
11 18624296 intron variant C/A;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs11082304
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs11209718
rs11209718
SCMH1
1 41223266 intron variant C/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs11259936
rs11259936
ADAMTSL3
15 83911830 intron variant A/C;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs1129923
rs1129923
DUSP23 ; LOC101928264
1 159782276 missense variant G/A;T snv 8.5E-02; 4.0E-06
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs115106883
rs115106883
SYN3 ; LOC105373002
22 32663679 intron variant G/C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011