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: 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: 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: 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: 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: rs1107748
rs1107748
1.000 0.080 17 43696446 intron variant T/C snv 0.54
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs12568930
rs12568930
1.000 0.040 1 22375738 intergenic variant T/C snv 0.21
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs12742784
rs12742784
1.000 0.080 1 22355873 intergenic variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2018
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: rs1905786
rs1905786
1.000 0.040 8 118939453 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2016266
rs2016266
SP7
1.000 0.080 12 53334171 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2012
dbSNP: rs2062305
rs2062305
1.000 0.040 13 42478744 intron variant G/A snv 0.46
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2062375
rs2062375
1.000 0.080 8 118965553 intergenic variant G/C snv 0.65
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2450083
rs2450083
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: rs3020348
rs3020348
1.000 0.040 6 151736779 intron variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs3757322
rs3757322
1.000 0.080 6 151621059 3 prime UTR variant T/G snv 0.36
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs4591859
rs4591859
1.000 0.080 6 151622504 downstream gene variant T/C snv 0.51
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs4869739
rs4869739
1.000 0.080 6 151580667 intron variant A/T snv 0.44
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 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: 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: rs7117858
rs7117858
1.000 0.080 11 15672916 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2009
dbSNP: rs7220711
rs7220711
1.000 0.080 17 43712597 intergenic variant A/G snv 0.52
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7328203
rs7328203
1.000 0.120 13 42414410 intron variant T/G snv 0.48
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7683315
rs7683315
1.000 0.080 4 87851943 intergenic variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7776340
rs7776340
1.000 0.080 6 151624531 downstream gene variant C/T snv 0.50
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009