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: rs387907351
rs387907351
CARD11 ; CARD11-AS1
1 1.000 7 2944495 missense variant T/C snv 7.0E-06 0.810 1.000 1 2019 2019
dbSNP: rs387907352
rs387907352
CARD11 ; CARD11-AS1
1 1.000 7 2944529 missense variant C/T snv 0.800 0
dbSNP: rs1554271741
rs1554271741
CARD11
2 0.925 7 2919373 stop gained G/A snv 0.700 0
dbSNP: rs571517554
rs571517554
CARD11 ; CARD11-AS1
1 1.000 7 2944528 missense variant C/T snv 0.700 0
dbSNP: rs794729673
rs794729673
CARD11
1 1.000 7 2947649 missense variant C/T snv 0.700 0