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: rs884205
rs884205
18 62387624 3 prime UTR variant A/C;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 4 2009 2018
dbSNP: rs13204965
rs13204965
6 126845927 intron variant A/C;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2011 2018
dbSNP: rs1346004
rs1346004
2 165744536 downstream gene variant G/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2012 2014
dbSNP: rs1524058
rs1524058
7 38096675 intergenic variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 2 2009 2018
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 2 2009 2012
dbSNP: rs2908004
rs2908004
1.000 0.040 7 121329715 missense variant G/A;T snv 0.44; 4.0E-06
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2012 2014
dbSNP: rs3801387
rs3801387
7 121334711 intron variant A/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2012 2018
dbSNP: rs754388
rs754388
0.882 0.120 14 92649065 intron variant G/C;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2014 2017
dbSNP: rs10005067
rs10005067
4 87931491 intergenic variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs10037512
rs10037512
5 89058858 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs10226308
rs10226308
7 37898820 intron variant A/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2012 2012
dbSNP: rs10788264
rs10788264
10 122256471 downstream gene variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
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: rs11023784
rs11023784
11 15925903 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs1124268
rs1124268
7 37945408 intron variant A/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs113306449
rs113306449
11 35959602 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs118115924
rs118115924
12 48985754 downstream gene variant G/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs12201899
rs12201899
6 45330467 intron variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
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: rs1262476
rs1262476
6 126665850 intron variant A/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2014 2014
dbSNP: rs12706298
rs12706298
7 120939583 intergenic variant C/A;G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
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: rs1286079
rs1286079
14 90978818 intron variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs1286150
rs1286150
14 90998546 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018