ClinVar Miner

List of variants in gene FRMD7 reported as uncertain significance for congenital nystagmus

Included ClinVar conditions (48):

Abnormality of the nervous system; Nystagmus
Albinism; Nystagmus; Myopia
Astigmatism; Hamartoma of hypothalamus; Global developmental delay; Nystagmus; Hypermetropia; Opsoclonus
Autism; Global developmental delay; Autistic behavior; Micrognathia; Abnormal corpus callosum morphology; Nystagmus; Stereotypic movement disorder; Hypoplasia of the corpus callosum; Abnormal pinna morphology; Delayed speech and language development; Downslanted palpebral fissures; Proximal placement of thumb; Speech apraxia; Wide intermamillary distance; Microcephaly; Facial hypotonia; Generalized hypotonia; Abnormal cerebral white matter morphology; Downturned corners of mouth; Long toe; Moderate global developmental delay; Cerebral white matter hypoplasia; Long fingers
Autism; Global developmental delay; Nystagmus; Retinal dystrophy; Rod-cone dystrophy
Cataract; Nystagmus; Retinal dystrophy; High myopia
Cerebellar ataxia; Nystagmus; Cerebellar atrophy; Dysmetria; Slurred speech; Dysdiadochokinesis; Slightly reduced reflexes
Cerebellar ataxia; Spasticity; Nystagmus; Strabismus; Postaxial hand polydactyly; Postaxial foot polydactyly; Ventriculomegaly
Congenital cerebellar hypoplasia; Global developmental delay; Hypertonia; Nystagmus; Primary microcephaly
Congenital cerebellar hypoplasia; Seizure; Oligohydramnios; Nystagmus; Hypoplasia of the corpus callosum; Delayed gross motor development
Congenital nystagmus
Congenital ocular coloboma; Global developmental delay; Visual impairment; Nystagmus; Absent speech; Barrel-shaped chest; Kidney damage; Cerebellar vermis hypoplasia; Tremor; Pancreatitis; Cerebellar malformation; Peritonitis; Infantile muscular hypotonia; Intellectual disability, severe
Cryptorchidism; Esotropia; Plagiocephaly; Global developmental delay; Short stature; Inguinal hernia; Nystagmus; Attention deficit hyperactivity disorder
Developmental cataract; Nystagmus; Microcornea; Sclerocornea
Developmental cataract; Nystagmus; Microphthalmia; Microcornea
Dystonic disorder; Global developmental delay; Seizure; Nystagmus; Cerebellar cortical atrophy
Dystonic disorder; Nystagmus; Inability to walk
Epicanthus; Hypertelorism; Esotropia; High palate; Low-set ears; EEG abnormality; Iris coloboma; Nystagmus; Microphthalmia; Short neck; Amblyopia; Abnormality of visual evoked potentials; Lens subluxation
Epicanthus; Micrognathia; Posteriorly rotated ears; Hearing impairment; Feeding difficulties; Optic nerve hypoplasia; Tall stature; Nystagmus; Tracheomalacia; Stereotypic movement disorder; Abnormal facial shape; Delayed speech and language development; Depressed nasal bridge; Downslanted palpebral fissures; Short philtrum; Abnormality of eye movement; Impaired social interactions; Preaxial hand polydactyly; Decreased fetal movement; Broad toe; Generalized non-motor (absence) seizure; Ankle flexion contracture; Reduced visual acuity; Hypoplastic helices; 1-2 finger syndactyly; Intellectual disability, severe; Severe global developmental delay; Gastrostomy tube feeding in infancy; Thick vermilion border
Exudative retinopathy; Retinal detachment; Cataract; Nystagmus; Blindness; Rod-cone dystrophy; Progressive visual loss; Retinal exudate; Abnormality of retinal pigmentation; Monocular strabismus; Optic disc drusen
Global developmental delay; Diarrhea; Nystagmus; Retinal dystrophy; Severely reduced visual acuity; Developmental regression; Gastrointestinal dysmotility
Global developmental delay; Expressive language delay; Seizure; Failure to thrive; Feeding difficulties; Growth delay; Nystagmus; Cerebral visual impairment; Strabismus; Intellectual disability; Limb hypertonia; Inability to walk; Multifocal epileptiform discharges; Hypotonia
Global developmental delay; Expressive language delay; Seizure; Failure to thrive; Growth delay; Nystagmus; Strabismus; Developmental regression; Limb hypertonia; Inability to walk; Multifocal epileptiform discharges; EEG with generalized epileptiform discharges; Hypotonia
Global developmental delay; Nystagmus; Intellectual disability; Elbow flexion contracture; Knee flexion contracture; Cerebral hypomyelination; Hypotonia
Global developmental delay; Seizure; Cataract; Nystagmus; Strabismus; Abnormal thorax morphology; Intellectual disability
Global developmental delay; Seizure; Nystagmus; Microcephaly
Hypertelorism; Visual impairment; Nystagmus
Hypotelorism; Low-set ears; Hypertonia; Nystagmus; Pointed chin; Protruding ear; Horizontal nystagmus; Anxiety; Phonophobia
Iris coloboma; Nystagmus; Generalized hypotonia; Cerebellar vermis hypoplasia
Leigh syndrome; Nystagmus; Lactic acidosis; Hypertrophic cardiomyopathy; Severe global developmental delay; Decreased activity of mitochondrial complex I
Leukodystrophy; Status epilepticus; Global developmental delay; Seizure; Fetal growth restriction; EEG abnormality; Nystagmus; Hemiparesis; Strabismus; Progressive visual loss; Amblyopia; Small for gestational age; Breech presentation; Neonatal hypoglycemia; Developmental regression; Loss of ambulation; EMG abnormality; EMG: axonal abnormality; Dysmyelinating leukodystrophy
Lissencephaly; Global developmental delay; Hypertonia; Nystagmus; Absent speech; Microcephaly; Strabismus
Motor delay; Seizure; Nystagmus; Abnormal facial shape; Absent speech; Delayed speech and language development; Myopia; Penile hypospadias; Recurrent otitis media; Retinal coloboma; Abnormal periventricular white matter morphology; Mild conductive hearing impairment; Severe global developmental delay
Nystagmus 1, congenital, X-linked
Nystagmus 1, congenital, X-linked; Simpson-Golabi-Behmel syndrome type 1
Nystagmus 6, congenital, X-linked
Nystagmus, congenital, autosomal recessive
Nystagmus; Abnormal electroretinogram
Nystagmus; Molar tooth sign on MRI; Central hypotonia
Nystagmus; Reduced eye contact; Ocular albinism
Ocular albinism, type I; Nystagmus 6, congenital, X-linked
Pectus excavatum; Nystagmus; Microcephaly; Hypotonia; visual disturbance
Persistent hyperplastic primary vitreous; Nystagmus; Short lingual frenulum; High myopia
Polydactyly; Nystagmus; Hypotonia
Pulmonary valve stenosis; Short stature; Failure to thrive; Scoliosis; Nystagmus; Microcephaly; Intellectual disability; Gray matter heterotopia; Parietal foramina; Proportionate short stature; Intellectual disability, severe
Seizure; Nystagmus; Dysarthria; Myoclonus; Tremor
Spastic ataxia; Choreoathetosis; Nystagmus; Dysarthria; Oculomotor apraxia; Intellectual disability; Cerebellar atrophy; Dysmetria; Tremor; Peripheral neuropathy
Spinocerebellar ataxia 27A

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_194277.3(FRMD7):c.*600C>G	rs750133372	0.00247
NM_194277.3(FRMD7):c.*573G>T	rs963218129	0.00064
NM_194277.3(FRMD7):c.1643A>C (p.Gln548Pro)	rs776519156	0.00012
NM_194277.3(FRMD7):c.*285C>T	rs766974170	0.00009
NM_194277.3(FRMD7):c.458G>A (p.Cys153Tyr)	rs199857416	0.00009
NM_194277.3(FRMD7):c.*196G>C	rs1057515770	0.00006
NM_194277.3(FRMD7):c.718A>G (p.Ile240Val)	rs773037705	0.00006
NM_194277.3(FRMD7):c.1481A>G (p.Gln494Arg)	rs199576118	0.00004
NM_194277.3(FRMD7):c.1799G>A (p.Arg600His)	rs751994722	0.00004
NM_194277.3(FRMD7):c.*300T>C	rs1029630139	0.00003
NM_194277.3(FRMD7):c.1200G>A (p.Ala400=)	rs61751728	0.00003
NM_194277.3(FRMD7):c.157A>G (p.Asn53Asp)	rs946251964	0.00003
NM_194277.3(FRMD7):c.1588C>T (p.Pro530Ser)	rs200651852	0.00003
NM_194277.3(FRMD7):c.992A>G (p.Gln331Arg)	rs773298405	0.00003
NM_194277.3(FRMD7):c.1646T>A (p.Val549Glu)	rs1308080722	0.00001
NM_194277.3(FRMD7):c.285-3C>T	rs750320516	0.00001
NM_194277.3(FRMD7):c.308A>C (p.Lys103Thr)	rs759784671	0.00001
NM_194277.3(FRMD7):c.58-6G>A	rs750979330	0.00001
NM_194277.3(FRMD7):c.*293G>C	rs1057515769
NM_194277.3(FRMD7):c.-100G>T	rs1057515772
NM_194277.3(FRMD7):c.-102G>A	rs1057515773
NM_194277.3(FRMD7):c.285-12A>G	rs1486391487
NM_194277.3(FRMD7):c.384A>G (p.Ser128=)	rs1927977937
NM_194277.3(FRMD7):c.810T>G (p.Thr270=)
NM_194277.3(FRMD7):c.904A>C (p.Ser302Arg)	rs1057515771

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