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: rs281875331
rs281875331
ACTB
1 1.000 0.240 7 5529624 missense variant T/C;G snv 0.800 1.000 2 2012 2015
dbSNP: rs281875332
rs281875332
ACTB
1 1.000 0.240 7 5529331 missense variant G/A;C snv 0.800 1.000 2 2012 2015
dbSNP: rs281875333
rs281875333
ACTB
1 1.000 0.240 7 5528497 missense variant G/A;T snv 0.800 1.000 2 2012 2015
dbSNP: rs281875334
rs281875334
ACTB
1 1.000 0.240 7 5528496 missense variant C/T snv 0.800 1.000 1 2012 2012
dbSNP: rs368352689
rs368352689
ACTB
1 1.000 0.240 7 5527786 missense variant C/G;T snv 4.0E-06 0.700 1.000 1 1999 1999
dbSNP: rs397515470
rs397515470
ACTB
2 0.925 0.280 7 5529175 missense variant C/T snv 0.700 1.000 1 2015 2015
dbSNP: rs587779769
rs587779769
ACTB
1 1.000 0.240 7 5529315 missense variant G/A snv 0.700 1.000 1 2015 2015
dbSNP: rs587779770
rs587779770
ACTB
1 1.000 0.240 7 5529304 missense variant C/T snv 0.700 1.000 1 2015 2015
dbSNP: rs587779771
rs587779771
ACTB
1 1.000 0.240 7 5529300 missense variant A/G snv 0.700 1.000 1 2015 2015
dbSNP: rs587779773
rs587779773
ACTB
1 1.000 0.240 7 5529168 missense variant A/G snv 0.700 1.000 1 2015 2015
dbSNP: rs587779774
rs587779774
ACTB
1 1.000 0.240 7 5529165 missense variant G/A snv 0.700 1.000 1 2015 2015
dbSNP: rs587779775
rs587779775
ACTB
1 1.000 0.240 7 5528637 missense variant G/A snv 0.700 1.000 1 2015 2015
dbSNP: rs587779776
rs587779776
ACTB
1 1.000 0.240 7 5528472 missense variant G/C snv 0.700 1.000 1 2015 2015
dbSNP: rs587779777
rs587779777
ACTB
1 1.000 0.240 7 5528458 missense variant C/T snv 0.700 1.000 1 2015 2015
dbSNP: rs104894003
rs104894003
ACTB
7 0.827 0.320 7 5528536 missense variant G/A snv 0.700 0
dbSNP: rs1166509821
rs1166509821
ACTB
2 0.925 0.240 7 5529305 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs1554329068
rs1554329068
ACTB
1 1.000 0.240 7 5527759 stop gained T/A snv 0.700 0
dbSNP: rs1554329113
rs1554329113
ACTB
1 1.000 0.240 7 5527863 missense variant G/A snv 0.700 0
dbSNP: rs1554329269
rs1554329269
ACTB
1 1.000 0.240 7 5528281 missense variant C/G snv 0.700 0
dbSNP: rs1554329331
rs1554329331
ACTB
1 1.000 0.240 7 5528556 missense variant A/G snv 0.700 0
dbSNP: rs1554329516
rs1554329516
ACTB
1 1.000 0.240 7 5529174 missense variant T/A snv 0.700 0
dbSNP: rs1554329523
rs1554329523
ACTB
1 1.000 0.240 7 5529195 frameshift variant A/- del 0.700 0
dbSNP: rs1554329546
rs1554329546
ACTB
1 1.000 0.240 7 5529253 inframe deletion AAG/- delins 0.700 0
dbSNP: rs1554329646
rs1554329646
ACTB
1 1.000 0.240 7 5529545 missense variant G/A snv 0.700 0
dbSNP: rs1562720119
rs1562720119
ACTB
1 1.000 0.240 7 5529639 missense variant C/T snv 0.700 0