ClinVar Miner

Variants in gene RP1L1 with conflicting interpretations "likely pathogenic" and "risk factor"

Submission 1 (likely pathogenic) minimum review status: Submission 1 (likely pathogenic) method:
Submission 2 (risk factor) minimum review status: Submission 2 (risk factor) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP
NM_178857.6(RP1L1):c.133C>T (p.Arg45Trp) rs267607017

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