NM_014339.7(IL17RA):c.138+87G>T AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003488891.2
Allele description [Variation Report for NM_014339.7(IL17RA):c.138+87G>T]
NM_014339.7(IL17RA):c.138+87G>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 23, 2024