ClinVar Miner

Variants in gene combination LOC100507346, PTCH1 with conflicting interpretations reported as "uncertain significance and "uncertain significance"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP
NM_001083602.2(PTCH1):c.2287G>A (p.Val763Met) rs201125580

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