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: 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: 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: rs10799445
rs10799445 		1 227724182 upstream gene variant A/C snv 0.27
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs10863936
rs10863936
DTL
1 212064456 intron variant G/A snv 0.59
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: rs11118346
rs11118346 		1 219570377 intergenic variant C/T snv 0.38
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs11205303
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29
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: 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: rs11809207
rs11809207
CATSPER4
1 26194649 intron variant G/A snv 0.19
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2009 2009
dbSNP: rs12075079
rs12075079
DNM3
1 172250855 intron variant A/G snv 0.16
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs12145922
rs12145922
PKN2-AS1
1 88680551 intron variant C/A snv 0.57
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs12735613
rs12735613 		1 118341350 intergenic variant G/A snv 0.22
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs1325598
rs1325598
PAPPA2
1 176823113 intron variant A/G snv 0.62
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs1390401
rs1390401
ZNF678
1 227610249 intron variant A/G snv 0.24
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs17038182
rs17038182 		1 118325782 intergenic variant G/C snv 0.25
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2009 2009
dbSNP: rs17346452
rs17346452
DNM3
1 172084147 intron variant T/C snv 0.19
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs1738475
rs1738475 		1 23210398 regulatory region variant C/G snv 0.49
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs17391694
rs17391694 		0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs2046159
rs2046159
COL24A1
1 85864906 intron variant A/G snv 0.13
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs2154319
rs2154319 		1 41280098 intron variant T/C snv 0.15
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs2274432
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs2421992
rs2421992
DNM3
1 172272111 intron variant C/T snv 0.62
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs3738814
rs3738814
ATP13A2
1 17005181 intron variant A/G snv 0.52
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010