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: rs884205
rs884205
TNFRSF11A
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: rs9533090
rs9533090
LINC02341
13 42377313 intron variant C/T snv 0.39
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 4 2009 2018
dbSNP: rs11898505
rs11898505
SPTBN1
2 54457420 intron variant A/G snv 0.76
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 3 2008 2018
dbSNP: rs1366594
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 3 2009 2018
dbSNP: rs2062377
rs2062377
COLEC10
8 118995181 upstream gene variant T/A snv 0.67
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 3 2009 2013
dbSNP: rs1038304
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2008 2009
dbSNP: rs11995824
rs11995824
COLEC10
8 119000461 intron variant C/G snv 0.65
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2009 2018
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: rs9594738
rs9594738
LINC02341
13 42378009 intron variant C/T snv 0.39
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2008 2018
dbSNP: rs9594759
rs9594759
LINC02341
13 42458457 intron variant C/T snv 0.51
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 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: rs1007738
rs1007738
CKAP5
11 46827809 intron variant G/A snv 0.64
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 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: 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: rs12407028
rs12407028
WLS ; GNG12-AS1
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: 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
WLS ; GNG12-AS1
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
WLS ; GNG12-AS1
1 68169392 intron variant T/C snv 0.18
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
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: rs1513670
rs1513670 		17 43729963 intergenic variant T/C snv 0.63
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs16921914
rs16921914
DCDC1
11 31189224 intron variant G/A snv 0.22
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs1999805
rs1999805
ESR1
1.000 0.120 6 151747229 intron variant G/A snv 0.55
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2008 2009
dbSNP: rs227584
rs227584
HROB
17 44148179 missense variant A/C snv 0.40 0.48
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009