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: rs9594759
rs9594759
13 42458457 intron variant C/T snv 0.51
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs9594738
rs9594738
13 42378009 intron variant C/T snv 0.39
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 2 2008 2018
dbSNP: rs2062305
rs2062305
1.000 0.040 13 42478744 intron variant G/A snv 0.46
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2017
dbSNP: rs9533090
rs9533090
13 42377313 intron variant C/T snv 0.39
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2018
dbSNP: rs9533090
rs9533090
13 42377313 intron variant C/T snv 0.39
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test
0.700 1.000 3 2012 2014
dbSNP: rs7992970
rs7992970
13 42371327 intron variant A/G snv 0.26
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2009 2009
dbSNP: rs10507508
rs10507508
13 42395646 intron variant A/G snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs10507509
rs10507509
13 42398954 intron variant C/T snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs11840862
rs11840862
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
13 42348370 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs12429224
rs12429224
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
13 42457891 intron variant T/C snv 0.43
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs12854504
rs12854504
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: rs12873631
rs12873631
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
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: rs1324003
rs1324003
13 42401990 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs1475249
rs1475249
13 42380369 intron variant A/G snv 0.26
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs17063206
rs17063206
13 42343323 intron variant C/T snv 0.16
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs17457561
rs17457561
13 42390067 intron variant G/A snv 0.21
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs17638544
rs17638544
13 42382485 intron variant C/T snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs180851
rs180851
13 42359904 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs1853573
rs1853573
13 42460832 intron variant G/C;T snv 0.46
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2062305
rs2062305
1.000 0.040 13 42478744 intron variant G/A snv 0.46
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs238252
rs238252
13 42341518 intron variant C/G snv 0.17
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs238255
rs238255
13 42349225 intron variant G/A snv 0.42
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009