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: rs1064797083
rs1064797083
FLI1
1 1.000 11 128810638 missense variant C/T snv 0.800 0
dbSNP: rs1064797084
rs1064797084
FLI1
1 1.000 11 128810657 missense variant A/G snv 0.800 0
dbSNP: rs1064797086
rs1064797086
FLI1
3 0.882 0.080 11 128810639 missense variant G/A snv 0.800 0
dbSNP: rs1064797087
rs1064797087
FLI1
2 0.925 0.040 11 128810662 missense variant A/G snv 0.800 0
dbSNP: rs773148506
rs773148506
FLI1
1 1.000 11 128810599 missense variant C/A;T snv 4.0E-06 0.800 0
dbSNP: rs1064797085
rs1064797085
FLI1
2 1.000 11 128810620 frameshift variant ATTA/- delins 0.700 0