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: rs3814333
rs3814333
COLGALT2
1 184037985 upstream gene variant C/T snv 0.29
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs425277
rs425277
PRKCZ
1 2137733 intron variant C/T snv 0.23
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs4338381
rs4338381
COL11A1
1.000 0.040 1 103107371 intron variant A/C;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs4601530
rs4601530 		1 24717620 downstream gene variant C/T snv 0.31
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs6662509
rs6662509
H6PD
1 9257545 intron variant C/T snv 0.17
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs6684205
rs6684205
TGFB2
1 218436360 intron variant A/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs6686842
rs6686842
SCMH1
1 41065199 intron variant T/C snv 0.65
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs6699417
rs6699417
PKN2-AS1
1 88657760 intron variant C/T snv 0.61
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs678962
rs678962
DNM3
1 172220749 intron variant T/G snv 0.24
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs7532866
rs7532866
LIN28A
1 26415053 intron variant A/G snv 0.36
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs7534091
rs7534091 		1 118321993 intergenic variant A/G snv 0.23
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs7552186
rs7552186 		1 218821931 intergenic variant C/T snv 0.40
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs900
rs900
TGFB2 ; TGFB2-OT1
0.882 0.040 1 218441563 3 prime UTR variant A/T snv 0.33
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs9428104
rs9428104 		1 118312964 intergenic variant A/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs3791675
rs3791675
EFEMP1
1.000 0.040 2 55884174 intron variant C/T snv 0.20
CUI: C0489786
Disease: Height
Height 		0.700 1.000 4 2008 2010
dbSNP: rs3791679
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20
CUI: C0489786
Disease: Height
Height 		0.700 1.000 3 2008 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: rs10187066
rs10187066
ZNF142
2 218650036 intron variant A/G snv 0.45
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs1052483
rs1052483 		2 219069626 non coding transcript exon variant G/T snv 0.13
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs11684404
rs11684404
EIF2AK3
2 88625104 intron variant T/C snv 0.28
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs11891311
rs11891311
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A3
2 233730664 intron variant G/A snv 0.42
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs11895026
rs11895026
CENPO
2 24813989 intron variant C/A;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs12470505
rs12470505
CFAP65
2 219043647 upstream gene variant T/G snv 0.19
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs12474201
rs12474201 		2 46694146 upstream gene variant G/A snv 0.30
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs12612930
rs12612930
ZNF638
2 71298655 intron variant T/C snv 4.5E-02
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013