FOXF1, forkhead box F1, 2294

N. diseases: 135; N. variants: 7
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs761162914
rs761162914
1.000 0.080 16 86512933 missense variant C/T snv 8.0E-06
Persistent Fetal Circulation Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases 0.700 1.000 3 2009 2016
dbSNP: rs121909336
rs121909336
1.000 0.080 16 86510794 stop gained C/A snv
Persistent Fetal Circulation Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases 0.700 0
dbSNP: rs121909337
rs121909337
1.000 0.080 16 86513083 stop lost T/C snv
Persistent Fetal Circulation Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases 0.700 0
dbSNP: rs1567511932
rs1567511932
1.000 0.080 16 86513085 stop lost A/C snv
Persistent Fetal Circulation Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases 0.700 0