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: rs2010281
rs2010281
MARK3
14 103395985 intron variant G/A snv 0.26
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs3103969
rs3103969
SAMD12-AS1 ; LOC105375723
8 118847564 intron variant A/G snv 0.57
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs2035979
rs2035979
SAMD12-AS1 ; LOC105375723
8 118860200 intron variant A/G snv 0.41
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs3103995
rs3103995
SAMD12-AS1 ; LOC105375723
8 118860712 intron variant A/C snv 0.41
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs2055101
rs2055101
SAMD12-AS1
8 118874684 intron variant C/T snv 0.50
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 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: 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: rs4407910
rs4407910
SAMD12-AS1
8 118904878 intron variant A/G snv 0.34
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: 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: 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: rs4355801
rs4355801 		0.882 0.120 8 118911634 regulatory region variant A/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2008 2009
dbSNP: rs4319131
rs4319131
TNFRSF11B
8 118935412 intron variant A/G snv 0.33
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: rs1905786
rs1905786
TNFRSF11B
1.000 0.040 8 118939453 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs6469788
rs6469788
TNFRSF11B
8 118940511 intron variant A/C;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1485289
rs1485289
TNFRSF11B
8 118942040 intron variant G/A snv 0.60
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs7464496
rs7464496
TNFRSF11B
8 118942603 intron variant T/C snv 0.60
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs6415470
rs6415470
TNFRSF11B
8 118942872 intron variant G/A snv 0.67
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs7463176
rs7463176
TNFRSF11B
8 118945386 intron variant A/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: rs3134063
rs3134063
TNFRSF11B
8 118947418 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs6469789
rs6469789
TNFRSF11B
8 118948422 intron variant C/A;G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs2073618
rs2073618
TNFRSF11B ; COLEC10
0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs2073617
rs2073617
TNFRSF11B ; COLEC10
0.776 0.360 8 118952044 upstream gene variant G/A snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009