Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16856823 2 169343942 intron variant A/T snv 4.6E-02 3
rs147287428 2 169206713 missense variant C/T snv 2.7E-04 4.7E-04 2
rs200309784 2 169347589 intron variant AA/-;A;AAA;AAAA delins 2
rs4667594 2 169151996 intron variant T/A;C snv 2
rs35472707 2 169139071 intron variant C/T snv 4.1E-02 1
rs3770636 2 169346323 intron variant T/G snv 4.6E-02 1
rs3815573 2 169155942 intron variant A/G;T snv 1
rs57989581 2 169337949 intron variant C/A snv 2.6E-02 1
rs60641214 2 169342782 intron variant A/T snv 0.25 1
rs755631 2 169150430 intron variant A/C snv 0.49 1