ClinVar Miner

Submissions for variant NM_005012.4(ROR1):c.2207G>C (p.Arg736Thr) (rs1553163562)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000504579 SCV000598635 pathogenic Deafness, autosomal recessive 108 2017-09-13 no assertion criteria provided literature only

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