Source: GWASCAT

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: rs3791679
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 7 2008 2019
dbSNP: rs2284746
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 6 2010 2019
dbSNP: rs3791675
rs3791675
EFEMP1
1.000 0.040 2 55884174 intron variant C/T snv 0.20
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 6 2008 2019
dbSNP: rs2093210
rs2093210
C14orf39
1.000 0.040 14 60490561 intron variant C/T snv 0.45
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 5 2010 2019
dbSNP: rs4369779
rs4369779
CABLES1
18 23155444 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 5 2014 2019
dbSNP: rs606452
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 5 2012 2019
dbSNP: rs7466269
rs7466269
FUBP3
9 130588697 intron variant A/G snv 0.33
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 5 2008 2017
dbSNP: rs1490384
rs1490384 		6 126530014 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2019
dbSNP: rs1812175
rs1812175
HHIP ; HHIP-AS1
4 144653692 intron variant A/G snv 0.79
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2008 2019
dbSNP: rs2280470
rs2280470
ACAN
15 88852395 intron variant A/G snv 0.68
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2017
dbSNP: rs2871865
rs2871865
IGF1R ; IRAIN
15 98651667 intron variant C/G snv 0.21
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2019
dbSNP: rs4282339
rs4282339
SLIT3
5 168829235 intron variant G/A snv 0.18
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2019
dbSNP: rs6060369
rs6060369
UQCC1
20 35319358 intron variant T/C snv 0.49
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2008 2019
dbSNP: rs6570507
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2009 2019
dbSNP: rs6763931
rs6763931
ZBTB38
0.925 0.080 3 141383991 intron variant G/A snv 0.54
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2008 2019
dbSNP: rs6918981
rs6918981 		6 34270737 intron variant G/A snv 0.69
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2009 2019
dbSNP: rs10906982
rs10906982
ADAMTSL3
15 83899406 intron variant T/A snv 0.63
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2008 2019
dbSNP: rs10958476
rs10958476
PLAG1
8 56183249 intron variant T/C snv 0.16
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2008 2014
dbSNP: rs11144688
rs11144688
PCSK5
9 75927370 intron variant G/A snv 9.2E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2010 2014
dbSNP: rs11658329
rs11658329
MAP3K3 ; STRADA ; LOC101927898
17 63685671 intron variant G/C snv 0.39
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2011 2019
dbSNP: rs1415701
rs1415701
L3MBTL3
6 130024690 intron variant G/A snv 0.31
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2013 2019
dbSNP: rs17511102
rs17511102
CDC42EP3 ; LOC105374465
2 37733470 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2010 2019
dbSNP: rs1787200
rs1787200
DYM
18 49061284 intron variant G/A snv 0.71
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2011 2019
dbSNP: rs1991431
rs1991431
ZBTB38
3 141414608 intron variant G/A snv 0.50
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2013 2019
dbSNP: rs2282978
rs2282978
CDK6 ; LOC112268009
7 92635096 intron variant T/C snv 0.38
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2008 2009