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: rs1270901
rs1270901
SPATS2
12 49441462 intron variant G/A snv 0.97
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs11910328
rs11910328
LINC01700
21 38978818 upstream gene variant G/A snv 0.85
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs4811196
rs4811196
CTNNBL1
20 37841292 intron variant G/A snv 0.81
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2007 2007
dbSNP: rs498079
rs498079
EYA4
6 133241318 intron variant G/C snv 0.81
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs2531992
rs2531992
ADCY9
16 3971733 intron variant A/G snv 0.80
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2019 2019
dbSNP: rs1021188
rs1021188 		13 42541997 intergenic variant C/T snv 0.79
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2010 2013
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: rs10824760
rs10824760
LNCAROD ; LOC105378305
10 52665565 intron variant C/T snv 0.75
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs1373004
rs1373004
LNCAROD ; LOC105378305
10 52668065 intron variant T/G snv 0.75
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2012 2012
dbSNP: rs2130604
rs2130604 		6 126499415 intron variant T/G snv 0.75
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2014 2014
dbSNP: rs6510186
rs6510186
TSHZ3
19 31163709 intron variant T/C snv 0.75
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs271170
rs271170
LINC00326
6 132994665 intron variant T/C snv 0.74
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2013 2013
dbSNP: rs2873195
rs2873195
SMG6
17 2161408 intron variant A/T snv 0.74
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs921874
rs921874
FZD4-DT ; LOC105369422
11 87012962 intron variant A/C snv 0.74
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs2252865
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs7398996
rs7398996 		12 53265664 upstream gene variant C/T snv 0.72
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs7781370
rs7781370
SEM1 ; LOC105375411
7 96504219 intron variant T/C snv 0.72
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs1159798
rs1159798
LNCAROD ; LOC105378305
10 52652733 intron variant A/C snv 0.70
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs2414095
rs2414095
CYP19A1 ; MIR4713HG
15 51232095 intron variant A/G snv 0.69
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs2553773
rs2553773
LOC105376626
11 35062086 regulatory region variant C/G snv 0.69
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs273573
rs273573
DCDC1 ; LOC105376611
11 30889444 intron variant A/C snv 0.69
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs10735851
rs10735851 		12 53349280 upstream gene variant G/A snv 0.68
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs11934731
rs11934731 		4 87910097 intergenic variant G/A snv 0.67
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 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: rs3018362
rs3018362 		0.882 0.120 18 62414860 upstream gene variant A/G snv 0.67
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2008 2008