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: rs228769
rs228769
HDAC5 ; LOC105371789
17 44115817 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs2450083
rs2450083
COLEC10
1.000 0.080 8 119051303 intron variant T/C snv 0.59
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2014
dbSNP: rs2504063
rs2504063
ESR1 ; LOC107986529
6 151769572 intron variant A/G snv 0.50
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs2566755
rs2566755
WLS ; GNG12-AS1
1 68169707 intron variant T/C snv 0.19
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs2710057
rs2710057 		X 86937000 intergenic variant G/T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs2941740
rs2941740
ESR1
6 151688503 intron variant A/G snv 0.40
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs3018362
rs3018362 		0.882 0.120 18 62414860 upstream gene variant A/G snv 0.67
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2008 2008
dbSNP: rs3020333
rs3020333
ESR1
6 151689119 intron variant A/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2018
dbSNP: rs3130340
rs3130340
TSBP1-AS1
0.851 0.200 6 32276850 intron variant T/C snv 0.25
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2008 2008
dbSNP: rs4233949
rs4233949
LOC102724072
2 54432570 regulatory region variant C/A;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2012
dbSNP: rs4355801
rs4355801 		0.882 0.120 8 118911634 regulatory region variant A/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2008 2009
dbSNP: rs4424296
rs4424296
COLEC10
8 119001037 intron variant C/T snv 0.61
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2014
dbSNP: rs4729260
rs4729260
SEM1 ; LOC105375411
7 96488606 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs4869742
rs4869742
CCDC170
6 151586613 intron variant C/A;G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2012
dbSNP: rs4870044
rs4870044
CCDC170
1.000 0.080 6 151580274 intron variant C/T snv 0.44
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2008 2009
dbSNP: rs599083
rs599083
LRP5
11 68424878 intron variant T/G snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs6426749
rs6426749 		1.000 0.080 1 22384980 intergenic variant G/C snv 0.19
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs6465511
rs6465511
SEM1 ; LOC105375411
7 96504803 intron variant C/A;G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2018
dbSNP: rs6469804
rs6469804
COLEC10
8 119032590 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2008 2009
dbSNP: rs6532023
rs6532023 		1.000 0.080 4 87852697 regulatory region variant T/G snv 0.66
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2012
dbSNP: rs6684375
rs6684375 		1 22379941 regulatory region variant C/T snv 0.20
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2017
dbSNP: rs6696981
rs6696981 		1 22376365 regulatory region variant G/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs6909279
rs6909279
CCDC170
6 151574321 intron variant G/C;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2013
dbSNP: rs6929137
rs6929137
CCDC170 ; LOC107986528
0.851 0.160 6 151615542 missense variant G/A snv 0.31 0.36
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs6959212
rs6959212 		7 38088724 intergenic variant T/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2012