ClinVar Miner

Submissions for variant NM_014026.6(DCPS):c.315G>A (p.Gln105=)

gnomAD frequency: 0.87290  dbSNP: rs637462
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001661374 SCV001876578 benign Al-Raqad syndrome 2021-07-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707666 SCV005231242 benign not provided criteria provided, single submitter not provided

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