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: rs11842146
rs11842146
13 42348370 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs1324003
rs1324003
13 42401990 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs180851
rs180851
13 42359904 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7992415
rs7992415
13 42401161 intron variant A/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs9533089
rs9533089
13 42376876 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs9533093
rs9533093
13 42387461 intron variant T/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs9533100
rs9533100
13 42422412 intron variant G/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7998154
rs7998154
13 42349255 intron variant T/C snv 1.8E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7338012
rs7338012
13 42359990 intron variant A/C snv 5.9E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10507508
rs10507508
13 42395646 intron variant A/G snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs12854504
rs12854504
13 42409565 intron variant T/G snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7987211
rs7987211
13 42392598 intron variant T/C snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7987728
rs7987728
13 42392876 intron variant T/A;C snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs12873631
rs12873631
13 42394260 intron variant T/C snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7994609
rs7994609
13 42394189 intron variant T/G snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7994209
rs7994209
13 42393993 intron variant T/C snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7992844
rs7992844
13 42394114 intron variant A/T snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7994236
rs7994236
13 42394042 intron variant T/C snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10507509
rs10507509
13 42398954 intron variant C/T snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7989519
rs7989519
13 42397078 intron variant A/G snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs12874234
rs12874234
13 42396587 intron variant A/G snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs7993166
rs7993166
13 42394027 intron variant G/A snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2875470
rs2875470
13 42399459 intron variant C/G snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs17638544
rs17638544
13 42382485 intron variant C/T snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs4454853
rs4454853
13 42399161 intron variant G/A snv 6.3E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009