Gene entry
PTCH2
patched 2
- Chromosome
- 1
- Cytoband
- 1p34.1
- Variants (rsID)
- 12
PTCH2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p34.1). Its official name is “patched 2”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs11573590Benignsingle nucleotide variantGorlin syndrome
- rs139624405Benignsingle nucleotide variantGorlin syndrome
- rs80168454Conflicting interpretationssingle nucleotide variantGorlin syndrome
- rs200366479Uncertain significancesingle nucleotide variantGorlin syndrome
- rs200800966Uncertain significancesingle nucleotide variantGorlin syndrome
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.