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: rs10808100
rs10808100
SEM1 ; LOC105375411
7 96501241 intron variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10872676
rs10872676 		6 151622842 downstream gene variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
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: rs10955908
rs10955908
SAMD12-AS1
8 118892318 intron variant C/A snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10955919
rs10955919
COLEC10
8 119008679 intron variant C/G snv 0.62
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10955924
rs10955924
COLEC10
8 119041104 intron variant C/A snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11155797
rs11155797
CCDC170
6 151580202 intron variant C/T snv 0.45
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11155811
rs11155811
ESR1
6 151756711 intron variant C/T snv 0.44
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: rs11573829
rs11573829
TNFRSF11B
8 118947384 intron variant T/A;C snv
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
dbSNP: rs11803476
rs11803476 		1 22376832 regulatory region variant C/T snv 0.15
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11810369
rs11810369 		1 22361158 downstream gene variant G/A snv 0.22
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11840862
rs11840862
LINC02341
13 42382327 intron variant A/G snv 0.56
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11842146
rs11842146
LINC02341
13 42348370 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11972702
rs11972702 		7 38108059 regulatory region variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11992136
rs11992136
COLEC10
8 118991488 upstream gene variant C/G snv 0.61
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 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 1 2009 2018
dbSNP: rs12197785
rs12197785 		6 151639470 intergenic variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs12197879
rs12197879
CCDC170
6 151574642 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 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: rs12429224
rs12429224
LINC02341
13 42457917 intron variant G/T snv 0.40
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs12430303
rs12430303
LINC02341
13 42457891 intron variant T/C snv 0.43
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs12561997
rs12561997 		1 22375787 TF binding site variant G/A snv 0.15
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
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