NM_000264.5(PTCH1):c.*1885G>A AND Holoprosencephaly 7
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001168179.4
Allele description [Variation Report for NM_000264.5(PTCH1):c.*1885G>A]
NM_000264.5(PTCH1):c.*1885G>A
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024