ClinVar Miner

Submissions for variant GRCh37/hg19 12q21.31(chr12:80696112-80696398)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GenomeConnect, ClinGen RCV001249215 SCV001423149 not provided Autosomal recessive nonsyndromic hearing loss 84B no assertion provided phenotyping only Variant interpretted as Uncertain significance and reported on 06-29-2018 by Lab or GTR ID 26957. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.

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