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: rs28584580
rs28584580
ACAN
15 88854596 intron variant A/G snv 0.11
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs28584580
rs28584580
ACAN
15 88854596 intron variant A/G snv 0.11
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs3784757
rs3784757
ACAN
1.000 0.040 15 88860173 intron variant G/A snv 0.13
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.020 1.000 2 2011 2014
dbSNP: rs3817428
rs3817428
ACAN
15 88872016 missense variant C/G snv 0.20 0.20
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs3817428
rs3817428
ACAN
15 88872016 missense variant C/G snv 0.20 0.20
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs3817428
rs3817428
ACAN
15 88872016 missense variant C/G snv 0.20 0.20
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2015 2015
dbSNP: rs35148461
rs35148461
ACAN
15 88870012 intron variant T/C snv 0.27
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2017 2019
dbSNP: rs1879529
rs1879529
ACAN
15 88871064 intron variant G/T snv 0.28
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs1879529
rs1879529
ACAN
15 88871064 intron variant G/T snv 0.28
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2017 2017
dbSNP: rs1879529
rs1879529
ACAN
15 88871064 intron variant G/T snv 0.28
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs8042988
rs8042988
ACAN
15 88869048 intron variant A/G snv 0.43
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2014 2019
dbSNP: rs1516797
rs1516797
ACAN
1.000 0.080 15 88867083 intron variant T/G snv 0.44
CUI: C0007286
Disease: Carpal Tunnel Syndrome
Carpal Tunnel Syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs2351491
rs2351491
ACAN
15 88854874 synonymous variant C/T snv 0.50 0.48
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs2351491
rs2351491
ACAN
15 88854874 synonymous variant C/T snv 0.50 0.48
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2011 2011
dbSNP: rs56071466
rs56071466
ACAN
15 88827235 intron variant G/A snv 0.50
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs938609
rs938609
ACAN
15 88855400 missense variant T/A snv 0.51 0.52
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs11633371
rs11633371
ACAN
15 88813601 intron variant G/T snv 0.53
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2280470
rs2280470
ACAN
15 88852395 intron variant A/G snv 0.68
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2017
dbSNP: rs2280470
rs2280470
ACAN
15 88852395 intron variant A/G snv 0.68
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs2280470
rs2280470
ACAN
15 88852395 intron variant A/G snv 0.68
CUI: C0455806
Disease: Infant length
Infant length 		0.700 1.000 1 2015 2015
dbSNP: rs11630187
rs11630187
ACAN
15 88844673 intron variant A/G snv 0.78
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019