VCV000866285.4 – ClinVar – NCBI

Likely pathogenic

(Feb 04, 2019)

criteria provided, single submitter

Method: clinical testing

Retinal dystrophy

Affected status: yes

Allele origin:

germline

Blueprint Genetics

Accession: SCV001239720.1

Submitted: (Oct 15, 2019)

Comment:

My Retina Tracker patient


Likely benign

(Dec 30, 2019)

criteria provided, single submitter

Method: clinical testing

not provided

Affected status: unknown

Allele origin:

germline

Invitae

Accession: SCV001602609.1

Submitted: (Jan 07, 2021)


Likely pathogenic

(Jan 06, 2021)

no assertion criteria provided

Method: clinical testing

Retinitis pigmentosa 7

Affected status: unknown

Allele origin:

germline

PerkinElmer Genomics

Accession: SCV002019063.1

Submitted: (Nov 19, 2021)


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