Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9940464
CDH13
1.000 0.040 16 83327170 intron variant T/C snv 0.39 1
rs8057927
CDH13
1.000 0.040 16 82659207 intron variant T/C snv 0.12 1
rs16957913
CDH13
16 82636644 intron variant T/C snv 3.7E-02 1
rs4783244
CDH13
0.925 0.120 16 82628663 intron variant G/T snv 0.38 1
rs7204454
CDH13
16 82625589 upstream gene variant G/C snv 0.59 1
rs12051272
CDH13
0.925 0.120 16 82629683 intron variant G/C;T snv 1
rs12597537
CDH13
16 82637031 intron variant A/G snv 8.1E-02 1
rs6565051
CDH13
16 82625123 upstream gene variant G/A snv 0.72 1
rs12599599
CDH13
16 82636934 intron variant G/A snv 3.4E-02 1
rs3096277
CDH13 ; LOC105371366
16 83730599 intron variant T/C snv 0.74 1