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: rs140727644
rs140727644
CFAP298 ; CFAP298-TCP10L
1 1.000 21 32604237 missense variant T/C snv 1.9E-04 1.9E-04 0.700 0
dbSNP: rs143740376
rs143740376
CFAP298 ; CFAP298-TCP10L
3 0.925 0.160 21 32609853 stop gained G/A snv 7.6E-05 8.4E-05 0.700 0
dbSNP: rs202094637
rs202094637
CFAP298 ; CFAP298-TCP10L
3 0.925 0.160 21 32602299 stop gained G/A;C snv 4.0E-06; 8.0E-05 0.700 0
dbSNP: rs398122401
rs398122401
CFAP298 ; CFAP298-TCP10L
2 0.925 0.160 21 32601941 frameshift variant AATA/- delins 4.0E-06 0.700 0