ClinVar Miner

Variants in gene USH2A with conflicting interpretations "likely pathogenic" and "benign"

Submission 1 (likely pathogenic) minimum review status: Submission 1 (likely pathogenic) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_206933.2(USH2A):c.3902G>T (p.Gly1301Val) rs111033524 0.00008

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