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: rs1038304
rs1038304
0.882 0.160 6 151612040 intron variant A/G snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs1999805
rs1999805
1.000 0.120 6 151747229 intron variant G/A snv 0.55
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs4870044
rs4870044
1.000 0.080 6 151580274 intron variant C/T snv 0.44
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs6469804
rs6469804
8 119032590 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs6993813
rs6993813
1.000 0.080 8 119039999 intron variant T/C snv 0.60
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs7524102
rs7524102
0.882 0.160 1 22371954 intergenic variant A/G snv 0.21
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2011
dbSNP: rs9594759
rs9594759
13 42458457 intron variant C/T snv 0.51
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs11898505
rs11898505
2 54457420 intron variant A/G snv 0.76
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 2 2008 2018
dbSNP: rs1564860
rs1564860
8 118963431 intergenic variant C/T snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2009 2009
dbSNP: rs2504063
rs2504063
6 151769572 intron variant A/G snv 0.50
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 2 2009 2009
dbSNP: rs3020331
rs3020331
6 151687645 intron variant C/T snv 0.38
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2009 2009
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 2 2008 2009
dbSNP: rs6469792
rs6469792
8 118996132 intron variant T/C snv 0.62
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2009 2009
dbSNP: rs6696981
rs6696981
1 22376365 regulatory region variant G/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 2 2009 2009
dbSNP: rs6929137
rs6929137
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 2 2009 2009
dbSNP: rs7752591
rs7752591
6 151625933 downstream gene variant G/A snv 0.56
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2009 2009
dbSNP: rs7753676
rs7753676
6 151555680 intron variant G/A snv 0.48
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2009 2009
dbSNP: rs7992970
rs7992970
13 42371327 intron variant A/G snv 0.26
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2009 2009
dbSNP: rs9594738
rs9594738
13 42378009 intron variant C/T snv 0.39
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 2 2008 2018
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
11 46827809 intron variant G/A snv 0.64
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2009
dbSNP: rs10085588
rs10085588
1.000 0.080 7 96508362 intron variant A/G snv 0.72
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10086835
rs10086835
8 119027942 intron variant C/T snv 0.63
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10091277
rs10091277
8 119022148 intron variant A/G snv 0.53
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10098408
rs10098408
8 119027482 intron variant T/C snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009