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: rs12723796
rs12723796 		1 22365113 non coding transcript exon variant G/A snv 0.16
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs12733835
rs12733835
WLS ; GNG12-AS1
1 68157311 intron variant C/A snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs12750721
rs12750721 		1 22362780 downstream gene variant G/A snv 0.22
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs12756978
rs12756978 		1 22358262 intergenic variant G/C snv 0.20
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: rs12861586
rs12861586 		13 42336328 upstream gene variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs12873631
rs12873631
LINC02341
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: rs12874234
rs12874234
LINC02341
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: rs12932673
rs12932673 		16 86676125 regulatory region variant C/G;T snv 0.16
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: rs1324003
rs1324003
LINC02341
13 42401990 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs13250753
rs13250753
SAMD12-AS1
8 118894453 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs13262276
rs13262276
COLEC10
8 119021679 intron variant T/A;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs13264172
rs13264172
COLEC10
8 119000622 intron variant T/A;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs13264791
rs13264791
COLEC10
8 119000851 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs13277230
rs13277230 		8 118910754 downstream gene variant C/T snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1336981
rs1336981
ESR1
6 151761234 intron variant C/T snv 0.74
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs13439134
rs13439134 		8 118906629 downstream gene variant G/C snv 0.34
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: rs1367447
rs1367447
WLS ; GNG12-AS1
1 68168347 intron variant C/T snv 0.17
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1385499
rs1385499
COLEC10
8 118962469 regulatory region variant G/A snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1403987
rs1403987 		7 38072339 intergenic variant A/G snv 0.63
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1403988
rs1403988 		7 38070334 regulatory region variant A/G snv 0.65
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1415193
rs1415193
ESR1 ; LOC107986529
6 151771503 intron variant T/A snv 0.37
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1415194
rs1415194
ESR1
6 151742863 intron variant A/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009