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: rs1787200
rs1787200
DYM
2 18 49061284 intron variant G/A snv 0.71 0.700 1.000 3 2011 2019
dbSNP: rs16950303
rs16950303
DYM
1 18 49055989 intron variant A/G snv 0.12 0.700 1.000 2 2015 2019
dbSNP: rs9967417
rs9967417
DYM
2 18 49433130 intron variant G/C;T snv 0.700 1.000 2 2010 2013
dbSNP: rs11659570
rs11659570
DYM
1 18 49320739 intron variant C/T snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs11664336
rs11664336
DYM
1 18 49078481 intron variant A/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs117406288
rs117406288
DYM
1 18 49250518 intron variant C/T snv 1.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs12458127
rs12458127
DYM
1 18 49130988 intron variant C/T snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs2878902
rs2878902
DYM
1 18 49124067 intron variant G/T snv 0.67 0.700 1.000 1 2017 2017
dbSNP: rs71355378
rs71355378
DYM
1 18 49292340 intron variant A/G snv 3.8E-02 0.700 1.000 1 2017 2017