ClinVar Miner

Submissions for variant NM_001184.4(ATR):c.1885+65ATTT[8]

dbSNP: rs56661838
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987345 SCV001136620 benign Seckel syndrome 1 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001712835 SCV001943591 benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000987345 SCV003801815 benign Seckel syndrome 1 2023-02-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003127561 SCV003801817 benign Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome 2023-02-08 criteria provided, single submitter clinical testing

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