ClinVar Miner

List of variants in gene ROBO4 reported as uncertain significance for familial bicuspid aortic valve

Included ClinVar conditions (18):

Adams-Oliver syndrome 2; Aortic valve disorder
Adams-Oliver syndrome 5; Aortic valve disorder
Aortic valve disease 1
Aortic valve disease 1; Adams-Oliver syndrome 5
Aortic valve disease 1; Familial thoracic aortic aneurysm and aortic dissection
Aortic valve disease 2
Aortic valve disease 2; Craniosynostosis 7
Aortic valve disease 3
Ascending tubular aorta aneurysm; Bicuspid aortic valve
Bicuspid aortic valve
Cardiac arrhythmia; Sudden cardiac death; Ventricular fibrillation; Aortic dilatation; Bicuspid aortic valve
Cryptorchidism; Triphalangeal thumb; Inguinal hernia; Feeding difficulties; Hemivertebrae; Constipation; Oligohydramnios; Hydroureter; Abnormal facial shape; Penile hypospadias; Strabismus; Intellectual disability; Generalized hypotonia; Mitral stenosis; Fetal pyelectasis; Patent ductus arteriosus after premature birth; Perimembranous ventricular septal defect; Neurodevelopmental delay; Bicuspid aortic valve
Epicanthus; Hypertelorism; Coarctation of aorta; Global developmental delay; Inguinal hernia; Bilateral cryptorchidism; Downslanted palpebral fissures; Short neck; Thin vermilion border; Wide intermamillary distance; Wide nose; Penile hypospadias; Low-set, posteriorly rotated ears; Thickened helices; Strabismus; Abnormal number of hair whorls; Bicuspid aortic valve; Smooth philtrum
Hereditary palmoplantar keratoderma; Bicuspid aortic valve
Migraine; Atrial septal defect, ostium secundum type; Rectal prolapse; Stress urinary incontinence; Bicuspid aortic valve
Narrow palate; Abnormal vena cava morphology; Aortic tortuosity; Bicuspid aortic valve
Radioulnar synostosis; Aortic valve disease 2
Radioulnar synostosis; Heart, malformation of; Bicuspid aortic valve

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_019055.6(ROBO4):c.691T>A (p.Tyr231Asn)	rs149517154	0.00027
NM_019055.6(ROBO4):c.190C>T (p.Arg64Cys)	rs201393279	0.00019
NM_019055.6(ROBO4):c.1471C>T (p.Arg491Cys)	rs374471211	0.00010
NM_019055.6(ROBO4):c.1702C>T (p.Arg568Ter)	rs201492213	0.00004
NM_019055.6(ROBO4):c.1529A>T (p.Asp510Val)	rs1565325937
NM_019055.6(ROBO4):c.1678C>T (p.Arg560Cys)
NM_019055.6(ROBO4):c.184A>G (p.Thr62Ala)
NM_019055.6(ROBO4):c.1900C>T (p.Arg634Cys)
NM_019055.6(ROBO4):c.2092C>A (p.Leu698Met)
NM_019055.6(ROBO4):c.2182C>T (p.Gln728Ter)
NM_019055.6(ROBO4):c.2758G>A (p.Gly920Ser)
NM_019055.6(ROBO4):c.746T>C (p.Leu249Pro)

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