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: rs104894203
rs104894203
RAD9A ; CLCF1 ; LOC100130987
2 0.925 0.200 11 67365224 missense variant C/A;T snv 0.800 1.000 1 2006 2006
dbSNP: rs104894198
rs104894198
RAD9A ; CLCF1 ; LOC100130987
2 0.925 0.200 11 67365493 stop gained G/A;T snv 8.0E-06 0.700 0
dbSNP: rs137853934
rs137853934
RAD9A ; CLCF1 ; LOC100130987
2 0.925 0.200 11 67367597 missense variant A/G snv 0.700 0