Gene: ACTG1 ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11549190
rs11549190
ACTG1 ; FSCN2
A 0.800 CausalMutation CLINVAR Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases. 25052316

2015
dbSNP: rs281875325
rs281875325
ACTG1 ; FSCN2
A 0.800 CausalMutation CLINVAR

dbSNP: rs281875326
rs281875326
ACTG1 ; FSCN2
A 0.800 CausalMutation CLINVAR

dbSNP: rs281875327
rs281875327
ACTG1 ; FSCN2
T 0.800 CausalMutation CLINVAR

dbSNP: rs281875328
rs281875328
ACTG1 ; FSCN2
A 0.800 CausalMutation CLINVAR

dbSNP: rs281875329
rs281875329
ACTG1 ; FSCN2
A 0.800 CausalMutation CLINVAR

dbSNP: rs1057518673
rs1057518673
ACTG1 ; FSCN2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs11549196
rs11549196
ACTG1 ; FSCN2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs587780275
rs587780275
ACTG1 ; FSCN2
T 0.700 GeneticVariation CLINVAR