Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7319172
PCDH9
13 66806036 intron variant G/A snv 0.50 1
rs12629751
PPARG
3 12357908 intron variant C/T snv 7.6E-02 1
rs2122127
PPP3R1
2 68218222 intron variant A/G snv 0.45 1