ClinVar Miner

Variants in gene combination LOC101927870, RELN with conflicting interpretations reported as "likely benign and "pathogenic"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (pathogenic) minimum review status: Submission 2 (pathogenic) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP
NM_005045.4(RELN):c.10093G>A (p.Val3365Ile) rs115035120

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