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: rs121908415
rs121908415
ACTN4 ; LOC107985291
2 0.925 0.080 19 38710286 missense variant A/G snv 7.0E-06 0.800 1.000 7 2000 2013
dbSNP: rs121908416
rs121908416
ACTN4 ; LOC107985291
2 0.925 0.080 19 38710299 missense variant C/T snv 0.800 1.000 7 2000 2013
dbSNP: rs121908417
rs121908417
ACTN4 ; LOC107985291
2 0.925 0.080 19 38710307 missense variant T/C snv 0.800 1.000 7 2000 2013
dbSNP: rs201128110
rs201128110
ACTN4 ; LOC107985291
1 1.000 0.080 19 38718062 missense variant G/A snv 1.7E-04 2.9E-04 0.700 1.000 7 2000 2013
dbSNP: rs112545413
rs112545413
ACTN4 ; LOC107985291
2 0.925 0.080 19 38717102 missense variant G/A snv 1.2E-02 9.6E-03 0.700 0
dbSNP: rs1568723797
rs1568723797
ACTN4 ; LOC107985291
1 1.000 0.080 19 38704994 missense variant T/C snv 0.700 0
dbSNP: rs1568725026
rs1568725026
ACTN4 ; LOC107985291
1 1.000 0.080 19 38706067 inframe deletion TCT/- delins 0.700 0
dbSNP: rs878853159
rs878853159
ACTN4 ; LOC107985291
1 1.000 0.080 19 38708128 missense variant G/A snv 0.700 0