Source: ALL

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: rs1856057
rs1856057
6 151746734 intron variant A/G snv 0.55
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs1890010
rs1890010
6 151764140 intron variant C/T snv 0.71
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs1999807
rs1999807
6 151743064 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs201941147
rs201941147
6 151735234 intron variant -/A ins
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2071454
rs2071454
6 151805689 5 prime UTR variant T/G snv 0.22
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2152750
rs2152750
6 151749010 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2206949
rs2206949
1.000 0.040 6 151716421 intron variant C/T snv 0.32
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.700 1.000 1 2017 2017
dbSNP: rs2504063
rs2504063
6 151769572 intron variant A/G snv 0.50
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test
0.700 1.000 1 2012 2012
dbSNP: rs2504065
rs2504065
6 151774032 intron variant G/A snv 0.47
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2504069
rs2504069
6 151764382 intron variant C/T snv 0.74
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2504071
rs2504071
6 151763727 intron variant T/C snv 0.47
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2747652
rs2747652
1.000 0.080 6 152115881 intron variant T/C snv 0.53
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.700 1.000 1 2017 2017
dbSNP: rs2941741
rs2941741
6 151687847 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982551
rs2982551
6 151740075 intron variant G/T snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982552
rs2982552
6 151738428 intron variant G/A snv 0.45
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982554
rs2982554
6 151736875 intron variant A/C snv 0.49
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982556
rs2982556
6 151735707 intron variant G/A snv 0.46
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982557
rs2982557
6 151735234 intron variant G/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982558
rs2982558
6 151735011 intron variant A/G snv 0.46
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982560
rs2982560
6 151734471 intron variant A/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982561
rs2982561
6 151731517 intron variant C/T snv 0.45
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982562
rs2982562
6 151731466 intron variant C/T snv 0.48
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982567
rs2982567
6 151754352 intron variant G/A snv 0.59
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982570
rs2982570
6 151692613 intron variant C/T snv 0.41
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs2982571
rs2982571
6 151691604 intron variant A/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009