ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.3109-27_3109-7dup

dbSNP: rs1555085333
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
Counsyl RCV000666662 SCV000790991 uncertain significance Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1 2017-04-18 criteria provided, single submitter clinical testing

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