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: rs17817600
rs17817600
1 1.000 0.080 11 85966428 intron variant A/G snv 9.7E-02 0.800 1.000 1 2012 2012
dbSNP: rs10501602
rs10501602
1 1.000 0.080 11 85970346 intron variant A/G snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs12787412
rs12787412
1 1.000 0.080 11 85992050 intron variant C/T snv 9.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs12790526
rs12790526
1 1.000 0.080 11 86056298 intron variant C/G snv 9.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs12794211
rs12794211
1 1.000 0.080 11 85992953 intron variant G/A snv 9.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs12795381
rs12795381
1 1.000 0.080 11 85993023 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs12795833
rs12795833
1 1.000 0.080 11 86002132 intron variant G/C snv 9.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs12802399
rs12802399
1 1.000 0.080 11 86045783 intron variant T/C snv 1.0E-01 0.700 1.000 1 2012 2012
dbSNP: rs17817648
rs17817648
1 1.000 0.080 11 85974242 intron variant T/C snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs17817931
rs17817931
1 1.000 0.080 11 86043772 intron variant T/C snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs17817992
rs17817992
1 1.000 0.080 11 86067709 intron variant C/T snv 9.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs527162
rs527162
1 1.000 0.080 11 86004693 intron variant C/T snv 0.82 0.700 1.000 1 2018 2018
dbSNP: rs639012
rs639012
1 1.000 0.080 11 85970540 intron variant A/G snv 0.72 0.700 1.000 1 2016 2016
dbSNP: rs867611
rs867611
1 1.000 0.080 11 86065502 intron variant G/A snv 0.73 0.700 1.000 1 2019 2019
dbSNP: rs11234495
rs11234495
1 1.000 0.080 11 85964391 intron variant C/T snv 0.23 0.010 1.000 1 2016 2016
dbSNP: rs588076
rs588076
1 1.000 0.080 11 85980619 intron variant G/A;C snv 0.010 < 0.001 1 2014 2014
dbSNP: rs592297
rs592297
2 0.925 0.080 11 86014894 synonymous variant C/T snv 0.78 0.82 0.010 1.000 1 2019 2019
dbSNP: rs676733
rs676733
1 1.000 0.080 11 86022967 intron variant C/T snv 0.72 0.010 1.000 1 2016 2016
dbSNP: rs677909
rs677909
1 1.000 0.080 11 86046547 intron variant C/T snv 0.72 0.010 1.000 1 2014 2014