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: rs1257763
rs1257763 		9 94131663 intron variant A/G snv 0.97
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs2401027
rs2401027
METTL25
12 82380120 intron variant T/C snv 0.92
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs2597513
rs2597513 		1.000 0.040 3 13514336 regulatory region variant C/T snv 0.88
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
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: rs6569648
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs1570106
rs1570106
RAD51B
14 68346398 intron variant T/C snv 0.84
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs6938239
rs6938239 		6 34715858 non coding transcript exon variant G/A snv 0.84
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs225694
rs225694
VTA1
6 142206005 intron variant A/G snv 0.83
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs2589113
rs2589113
CCDC88A
2 55289187 3 prime UTR variant T/G snv 0.83
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs6439167
rs6439167 		3 129331913 upstream gene variant T/C snv 0.82
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs2247056
rs2247056
HLA-B ; LINC02571 ; LOC112267902
0.882 0.160 6 31297713 intron variant T/C snv 0.80
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs2780226
rs2780226 		6 34231315 regulatory region variant C/T snv 0.80
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs1776897
rs1776897 		6 34227234 regulatory region variant G/T snv 0.80
CUI: C0489786
Disease: Height
Height 		0.700 1.000 3 2008 2010
dbSNP: rs1812175
rs1812175
HHIP ; HHIP-AS1
4 144653692 intron variant A/G snv 0.79
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2008 2010
dbSNP: rs7689420
rs7689420
HHIP ; HHIP-AS1
0.851 0.080 4 144647200 non coding transcript exon variant T/C snv 0.79
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs422421
rs422421
FGFR4
5 177090325 intron variant T/C snv 0.83 0.79
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs849141
rs849141
JAZF1
0.851 0.240 7 28145472 intron variant A/G snv 0.78
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2009 2009
dbSNP: rs6714546
rs6714546
LTBP1
2 33136358 intron variant A/G snv 0.78
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs606452
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2012 2012
dbSNP: rs634552
rs634552
SERPINH1
11 75571007 intron variant T/G snv 0.77
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs1708299
rs1708299
JAZF1
7 28150327 intron variant A/G snv 0.77
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs488133
rs488133
ESR1
6 151804309 intron variant T/C snv 0.77
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs3917210
rs3917210
TGFB3 ; IFT43
14 75961437 intron variant T/A snv 0.77
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs139909
rs139909
TNRC6B
22 40301577 intron variant C/T snv 0.74
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2009 2009
dbSNP: rs2707450
rs2707450
LCORL
4 17940937 intron variant C/T snv 0.73
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011