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: rs12568456
rs12568456
WLS ; GNG12-AS1
1 68195803 intron variant T/G snv 0.21
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs12854504
rs12854504
LINC02341
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: rs1293936
rs1293936
ESR1
6 151696556 intron variant T/G snv 0.45
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1357651
rs1357651 		7 38058260 intergenic variant T/G snv 0.64
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs3757322
rs3757322
CCDC170
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: rs4342521
rs4342521
SEM1 ; LOC105375411
7 96506693 missense variant T/G snv 0.72
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs599083
rs599083
LRP5
11 68424878 intron variant T/G snv 0.34
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: rs6984675
rs6984675
COLEC10
8 119032988 intron variant T/G snv 0.63
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs7328203
rs7328203
LINC02341
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: rs7607093
rs7607093
LOC102724072
2 54432037 regulatory region variant T/G snv 0.74
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs7994609
rs7994609
LINC02341
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: rs1124674
rs1124674
ESR1
6 151759600 intron variant T/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1524068
rs1524068 		7 38071024 regulatory region variant T/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs4869741
rs4869741
CCDC170
6 151585158 intron variant T/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs6959212
rs6959212 		7 38088724 intergenic variant T/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2012
dbSNP: rs7554551
rs7554551
WLS ; GNG12-AS1
1 68199340 intron variant T/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs9303521
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs9533093
rs9533093
LINC02341
13 42387461 intron variant T/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs6993813
rs6993813
COLEC10
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: rs6469792
rs6469792
COLEC10
8 118996132 intron variant T/C snv 0.62
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2009 2009
dbSNP: rs10098408
rs10098408
COLEC10
8 119027482 intron variant T/C snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
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: rs1107748
rs1107748
LINC02594
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: rs11573885
rs11573885
TNFRSF11B
8 118936926 intron variant T/C snv 0.45
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009