Source: ALL
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: rs121434539
rs121434539
CDH15
1 1.000 0.160 16 89179551 missense variant C/T snv 1.2E-04 7.7E-05 0.700 1.000 1 2008 2008
dbSNP: rs121434540
rs121434540
CDH15
1 1.000 0.160 16 89180272 missense variant C/T snv 5.4E-05 1.1E-04 0.700 0
dbSNP: rs121434541
rs121434541
CDH15
1 1.000 0.160 16 89183555 missense variant C/T snv 2.0E-04 6.6E-04 0.700 0
dbSNP: rs567903921
rs567903921
CDH15
1 1.000 0.160 16 89171853 missense variant G/C snv 1.3E-04 1.6E-04 0.700 0