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: rs794726858
rs794726858
CNNM2 ; LOC107984265
1 1.000 10 102919286 missense variant C/G snv 0.800 1.000 1 2014 2014
dbSNP: rs786205909
rs786205909
CNNM2 ; LOC107984265
1 1.000 10 102918844 missense variant G/A snv 4.9E-06 0.800 0
dbSNP: rs786205910
rs786205910
CNNM2 ; LOC107984265
1 1.000 10 102919549 missense variant G/A snv 0.800 0