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: rs10804515
rs10804515
ZBTB20
3 114983210 intron variant A/G snv 0.60
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2007 2007
dbSNP: rs1042725
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48
CUI: C0489786
Disease: Height
Height 		0.700 1.000 3 2007 2008
dbSNP: rs6060369
rs6060369
UQCC1
20 35319358 intron variant T/C snv 0.49
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2008 2008
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: rs10935120
rs10935120
CEP63
3 134514250 intron variant A/G snv 0.63
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs12198986
rs12198986 		6 7719826 regulatory region variant G/A snv 0.37
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs12199222
rs12199222
NUP153
1.000 0.040 6 17699091 intron variant G/A;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
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: rs12986413
rs12986413
DOT1L
19 2170955 intron variant A/T snv 0.46
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
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: rs1406948
rs1406948
UQCC1
20 35317816 intron variant G/A snv 0.44
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs1406949
rs1406949
UQCC1
20 35318101 intron variant C/A;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs143383
rs143383
GDF5
0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs1490388
rs1490388 		6 126514509 intron variant C/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs1492820
rs1492820
HHIP
4 144728869 intron variant G/A snv 0.50
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs16896068
rs16896068
LCORL
4 17943217 intron variant G/A snv 0.25
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs17690232
rs17690232 		4 54368658 regulatory region variant C/A;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs185819
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
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: rs2326458
rs2326458 		16 84954073 intergenic variant C/A snv 0.67
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs2554380
rs2554380 		15 83647132 intergenic variant C/T snv 0.85
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs2562784
rs2562784
SH3GL3
15 83617740 intron variant A/G snv 0.29
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs2730245
rs2730245
WDR60
7 158932098 intron variant G/A;C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs2814828
rs2814828 		9 88196267 intergenic variant T/A;C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs2814993
rs2814993
ILRUN
1.000 0.040 6 34651116 intron variant G/A snv 0.17
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008