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: rs10506701
rs10506701
LOC100507377
12 74192430 intron variant T/G snv 0.15
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2007 2007
dbSNP: rs2165468
rs2165468
LINC02669 ; LOC105376360
10 3473913 intron variant C/A snv 0.20
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2007 2007
dbSNP: rs4087296
rs4087296 		16 82344176 regulatory region variant T/C snv 0.26
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2007 2007
dbSNP: rs4811196
rs4811196
CTNNBL1
20 37841292 intron variant G/A snv 0.81
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2007 2007
dbSNP: rs9317284
rs9317284 		13 63060217 intron variant G/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2007 2007
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: 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: rs1038304
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2008 2009
dbSNP: rs9594759
rs9594759
LINC02341
13 42458457 intron variant C/T snv 0.51
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2008 2009
dbSNP: rs10048146
rs10048146 		1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs1007738
rs1007738
CKAP5
11 46827809 intron variant G/A snv 0.64
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs10876432
rs10876432
SP7
12 53338107 intron variant G/A snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs1430742
rs1430742
WLS ; GNG12-AS1
1 68169392 intron variant T/C snv 0.18
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs1471403
rs1471403 		1.000 0.080 4 87854091 intergenic variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs1513670
rs1513670 		17 43729963 intergenic variant T/C snv 0.63
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs16921914
rs16921914
DCDC1
11 31189224 intron variant G/A snv 0.22
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs16945612
rs16945612
ADAMTS18
16 77395075 intron variant T/C snv 0.13
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs17131547
rs17131547
TGFBR3
1 91745463 intron variant G/A snv 5.0E-02
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1999805
rs1999805
ESR1
1.000 0.120 6 151747229 intron variant G/A snv 0.55
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2008 2009
dbSNP: rs227584
rs227584
HROB
17 44148179 missense variant A/C snv 0.40 0.48
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
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: 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