ClinVar Miner

Submissions for variant NM_006343.3(MERTK):c.1866G>C (p.Lys622Asn)

dbSNP: rs775460185
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Genomic Medicine, Manchester, Central Manchester University Hospitals RCV000225485 SCV000282561 uncertain significance Retinal dystrophy no assertion criteria provided clinical testing

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