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: rs1366594
rs1366594
5 89080244 intron variant A/C snp 0.55
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 4 2009 2018
dbSNP: rs2062377
rs2062377
8 118995181 regulatory region variant T/A snp 0.66
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 4 2009 2014
dbSNP: rs7524102
rs7524102
0.923 0.143 1 22371954 intergenic variant A/G snp 0.20
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 4 2008 2011
dbSNP: rs9533090
rs9533090
13 42377313 intron variant C/T snp 0.40
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 4 2009 2018
dbSNP: rs10048146
rs10048146
16 86677054 intergenic variant A/G snp 0.18
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2009 2014
dbSNP: rs1038304
rs1038304
1.000 0.071 6 151612040 intron variant A/G snp 0.57
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2008 2009
dbSNP: rs1999805
rs1999805
6 151747229 intron variant G/A snp 0.57
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2008 2009
dbSNP: rs2504063
rs2504063
6 151769572 intron variant A/G snp 0.52
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2009 2012
dbSNP: rs3801387
rs3801387
7 121334711 intron variant A/C,G snp 0.29
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2012 2018
dbSNP: rs4355801
rs4355801
0.878 0.107 8 118911634 intergenic variant A/G,T snp 0.35; 1.6E-04
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2008 2009
dbSNP: rs4727338
rs4727338
7 96491363 intron variant G/C,T snp 0.72
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2009 2014
dbSNP: rs4869742
rs4869742
6 151586613 intron variant C/A,G,T snp 0.43
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2009 2014
dbSNP: rs4870044
rs4870044
1.000 0.071 6 151580274 intron variant C/T snp 0.44
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2008 2009
dbSNP: rs6426749
rs6426749
1 22384980 G/C snp 0.18
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2009 2014
dbSNP: rs6469804
rs6469804
8 119032590 intron variant G/A,C snp 0.67
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2008 2009
dbSNP: rs6993813
rs6993813
8 119039999 intron variant T/C snp 0.59
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2008 2009
dbSNP: rs9594759
rs9594759
13 42458457 intron variant C/T snp 0.52
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 3 2008 2009
dbSNP: rs1021188
rs1021188
13 42541997 intergenic variant C/T snp 0.80
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 2 2010 2013
dbSNP: rs11898505
rs11898505
2 54457420 intron variant A/G snp 0.77
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 2 2008 2018
dbSNP: rs12407028
rs12407028
1 68182033 intron variant T/C snp 0.36
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 2 2009 2012
dbSNP: rs13204965
rs13204965
6 126845927 intergenic variant A/C,T snp 0.17
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 2 2011 2018
dbSNP: rs13245690
rs13245690
7 121145010 intron variant A/G snp 0.32
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 2 2012 2017
dbSNP: rs1430740
rs1430740
1 68191827 intron variant T/C snp 0.61
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 2 2009 2014
dbSNP: rs2016266
rs2016266
SP7
12 53334171 intron variant G/A,C snp 0.62; 3.2E-05
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 2 2009 2012
dbSNP: rs227584
rs227584
17 44148179 missense variant A/C snp 0.40 0.48
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 2 2009 2012