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: rs746481984
rs746481984
CDH1
5 0.851 0.120 16 68819393 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs757422353
rs757422353
CDH1
3 0.882 0.200 16 68823432 missense variant C/G snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs876658146
rs876658146
CDH1
3 0.882 0.200 16 68815743 missense variant A/G snv 0.010 1.000 1 2019 2019
dbSNP: rs876659384
rs876659384
TP53
7 0.851 0.240 17 7673552 stop gained C/A snv 0.010 1.000 1 2004 2004