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: 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 4 2008 2011
dbSNP: rs34920465
rs34920465
0.807 0.160 1 22373858 intergenic variant A/G snv 0.24
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2014 2018
dbSNP: rs3765350
rs3765350
1 22120823 intron variant A/G snv 0.22
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2014 2017
dbSNP: rs10493013
rs10493013
1 22376542 regulatory region variant T/C snv 0.20
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2018
dbSNP: rs10737462
rs10737462
1 22118482 3 prime UTR variant C/T snv 0.22
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs12044944
rs12044944
1 240418353 intron variant C/T snv 0.18
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs12407028
rs12407028
1 68182033 intron variant T/A;C snv 0.35
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2012
dbSNP: rs12408576
rs12408576
1 40998765 intron variant A/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2019 2019
dbSNP: rs12741884
rs12741884
1 22268202 downstream gene variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2017 2017
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: rs1430740
rs1430740
1 68191827 intron variant T/C snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2014
dbSNP: rs1430742
rs1430742
1 68169392 intron variant T/C snv 0.18
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2009
dbSNP: rs17131547
rs17131547
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: rs185048405
rs185048405
1 219865483 intron variant C/T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs2235529
rs2235529
1.000 0.040 1 22123994 intron variant C/T snv 0.13
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2014 2014
dbSNP: rs2252865
rs2252865
0.851 0.040 1 8362616 intron variant T/C snv 0.72
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs2566752
rs2566752
1.000 0.080 1 68191014 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs2566755
rs2566755
1 68169707 intron variant T/C snv 0.19
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2009
dbSNP: rs3920498
rs3920498
1.000 0.040 1 22166394 intergenic variant G/C snv 0.19
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2014 2014
dbSNP: rs3971300
rs3971300
1 22158082 downstream gene variant T/C snv 0.33
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs4846580
rs4846580
1 219724599 intron variant G/A snv 0.40
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs56318008
rs56318008
0.925 0.120 1 22143914 5 prime UTR variant C/T snv 0.13
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs633995
rs633995
1 172217589 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
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: rs6679981
rs6679981
1 22371367 upstream gene variant G/A snv 0.21
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018