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: rs9533090
rs9533090
LINC02341
13 42377313 intron variant C/T snv 0.39
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 4 2009 2018
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: rs1366594
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 3 2009 2018
dbSNP: rs1038304
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2008 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 2 2009 2018
dbSNP: rs12272917
rs12272917
PPP6R3
11 68495902 intron variant T/C snv 0.23
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2014 2017
dbSNP: rs13204965
rs13204965 		6 126845927 intron variant A/C;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2011 2018
dbSNP: rs13245690
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2012 2017
dbSNP: rs2016266
rs2016266
SP7
1.000 0.080 12 53334171 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2009 2012
dbSNP: rs3765350
rs3765350
WNT4
1 22120823 intron variant A/G snv 0.22
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2014 2017
dbSNP: rs3801387
rs3801387
WNT16
7 121334711 intron variant A/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2012 2018
dbSNP: rs754388
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2014 2017
dbSNP: rs7776725
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2009 2014
dbSNP: rs8001611
rs8001611
LINC02341
13 42391558 intron variant C/T snv 0.59
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2013 2018
dbSNP: rs917727
rs917727
FAM3C
7 121378525 intron variant C/A;T snv 0.33
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2012 2017
dbSNP: rs9533095
rs9533095
LINC02341
13 42394913 intron variant G/T snv 0.39
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 2 2014 2018
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: rs9594759
rs9594759
LINC02341
13 42458457 intron variant C/T snv 0.51
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 2 2008 2009
dbSNP: rs10037512
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 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: rs10226308
rs10226308
NME8 ; EPDR1
7 37898820 intron variant A/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2012 2012
dbSNP: rs10416218
rs10416218
GPATCH1
19 33108221 intron variant T/C snv 0.42
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2012 2012
dbSNP: rs10429035
rs10429035
SEM1 ; LOC105375411
7 96490169 intron variant G/A snv 0.39
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2014 2014
dbSNP: rs10490046
rs10490046
SLC8A1
2 40403538 intron variant A/C snv 0.28
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs10506701
rs10506701
LOC100507377
12 74192430 intron variant T/G snv 0.15
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2007 2007