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: rs6469804
rs6469804
COLEC10
8 119032590 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 3 2008 2009
dbSNP: rs9594759
rs9594759
LINC02341
13 42458457 intron variant C/T snv 0.51
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 3 2008 2009
dbSNP: rs11898505
rs11898505
SPTBN1
2 54457420 intron variant A/G snv 0.76
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2008 2018
dbSNP: rs1564860
rs1564860
COLEC10
8 118963431 intergenic variant C/T snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2009 2009
dbSNP: rs2504063
rs2504063
ESR1 ; LOC107986529
6 151769572 intron variant A/G snv 0.50
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2009 2009
dbSNP: rs3020331
rs3020331
ESR1
6 151687645 intron variant C/T snv 0.38
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2009 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: rs6696981
rs6696981 		1 22376365 regulatory region variant G/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2009 2009
dbSNP: rs7752591
rs7752591 		6 151625933 downstream gene variant G/A snv 0.56
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2009 2009
dbSNP: rs7753676
rs7753676
CCDC170
6 151555680 intron variant G/A snv 0.48
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2009 2009
dbSNP: rs7992970
rs7992970
LINC02341
13 42371327 intron variant A/G snv 0.26
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2009 2009
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: 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: rs10086835
rs10086835
COLEC10
8 119027942 intron variant C/T snv 0.63
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10091277
rs10091277
COLEC10
8 119022148 intron variant A/G snv 0.53
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 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: rs10101385
rs10101385 		8 118911611 regulatory region variant A/G snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1023940
rs1023940
CCDC170 ; LOC107986528
6 151611643 intron variant A/G snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1036066
rs1036066
WLS ; GNG12-AS1
1 68194522 intron variant A/C snv 0.33
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10464592
rs10464592
SEM1
7 96601374 intron variant G/A snv 0.34
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: rs10505348
rs10505348
COLEC10
8 118960457 intergenic variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10505351
rs10505351
COLEC10
8 119021759 intron variant C/T snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10507508
rs10507508
LINC02341
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: rs10507509
rs10507509
LINC02341
13 42398954 intron variant C/T snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009