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: rs104894544
rs104894544
ACTG1 ; FSCN2
1 1.000 0.120 17 81511913 missense variant T/A;C snv 0.800 1.000 7 2003 2014
dbSNP: rs104894545
rs104894545
ACTG1
1 1.000 0.120 17 81510824 missense variant G/C snv 0.800 1.000 7 2003 2014
dbSNP: rs104894546
rs104894546
ACTG1 ; FSCN2
1 1.000 0.120 17 81511199 missense variant G/A snv 0.800 1.000 7 2003 2014
dbSNP: rs104894547
rs104894547
ACTG1
1 1.000 0.120 17 81510709 missense variant A/G snv 0.800 1.000 7 2003 2014
dbSNP: rs28999111
rs28999111
ACTG1 ; FSCN2
1 1.000 0.120 17 81512000 missense variant G/A snv 0.800 1.000 7 2003 2014
dbSNP: rs28999112
rs28999112
ACTG1 ; FSCN2
1 1.000 0.120 17 81511078 missense variant G/A snv 0.800 1.000 7 2003 2014
dbSNP: rs267606630
rs267606630
ACTG1 ; FSCN2
1 1.000 0.120 17 81511912 missense variant C/G;T snv 8.0E-06 0.800 0
dbSNP: rs267606631
rs267606631
ACTG1 ; FSCN2
1 1.000 0.120 17 81511269 missense variant C/T snv 0.800 0
dbSNP: rs281875330
rs281875330
ACTG1 ; FSCN2
2 1.000 0.120 17 81511626 missense variant T/C snv 0.700 1.000 7 2003 2014
dbSNP: rs281875329
rs281875329
ACTG1 ; FSCN2
3 0.925 0.120 17 81511224 missense variant G/A;T snv 4.0E-06 0.700 0