Gene: ACAN ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2280470
rs2280470
ACAN
3 15 88852395 intron variant A/G snv 0.68 0.700 1.000 4 2010 2017
dbSNP: rs16942341
rs16942341
ACAN
3 15 88845674 synonymous variant C/T snv 3.8E-02 6.4E-02 0.700 1.000 2 2010 2019
dbSNP: rs35148461
rs35148461
ACAN
1 15 88870012 intron variant T/C snv 0.27 0.700 1.000 2 2017 2019
dbSNP: rs8041863
rs8041863
ACAN
2 15 88816458 intron variant T/A;G snv 0.700 1.000 2 2008 2019
dbSNP: rs8042988
rs8042988
ACAN
1 15 88869048 intron variant A/G snv 0.43 0.700 1.000 2 2014 2019
dbSNP: rs11630187
rs11630187
ACAN
1 15 88844673 intron variant A/G snv 0.78 0.700 1.000 1 2019 2019
dbSNP: rs11633371
rs11633371
ACAN
1 15 88813601 intron variant G/T snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs16942323
rs16942323
ACAN
1 15 88840533 intron variant T/C snv 2.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs2351491
rs2351491
ACAN
2 15 88854874 synonymous variant C/T snv 0.50 0.48 0.700 1.000 1 2011 2011
dbSNP: rs28584580
rs28584580
ACAN
2 15 88854596 intron variant A/G snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs3817428
rs3817428
ACAN
3 15 88872016 missense variant C/G snv 0.20 0.20 0.700 1.000 1 2015 2015
dbSNP: rs4932200
rs4932200
ACAN
1 15 88806477 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs56071466
rs56071466
ACAN
1 15 88827235 intron variant G/A snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs56238630
rs56238630
ACAN
1 15 88842993 intron variant T/C snv 6.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs72765671
rs72765671
ACAN
1 15 88817911 intron variant A/G snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs938614
rs938614
ACAN
1 15 88811655 intron variant T/A;C snv 0.700 1.000 1 2017 2017