NM_025132.4(WDR19):c.961+2T>C AND multiple conditions
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Mar 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001043448.6
Allele description [Variation Report for NM_025132.4(WDR19):c.961+2T>C]
NM_025132.4(WDR19):c.961+2T>C
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024