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: rs387907072
rs387907072
MEGF10
2 0.925 5 127440825 missense variant T/C snv 1.6E-05 2.1E-05 0.700 0
dbSNP: rs387907073
rs387907073
MEGF10
2 0.925 5 127410447 missense variant T/C snv 0.700 0
dbSNP: rs387907074
rs387907074
MEGF10
2 0.925 5 127339214 missense variant C/T snv 2.4E-05 1.4E-05 0.700 0