Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11659570
DYM
18 49320739 intron variant C/T snv 0.31 1
rs11664336
DYM
18 49078481 intron variant A/T snv 0.32 1
rs117406288
DYM
18 49250518 intron variant C/T snv 1.1E-02 1
rs12458127
DYM
18 49130988 intron variant C/T snv 0.10 1
rs16950303
DYM
18 49055989 intron variant A/G snv 0.12 1
rs1787200
DYM
18 49061284 intron variant G/A snv 0.71 1
rs2878902
DYM
18 49124067 intron variant G/T snv 0.67 1
rs71355378
DYM
18 49292340 intron variant A/G snv 3.8E-02 1
rs9967417
DYM
18 49433130 intron variant G/C;T snv 1