NM_024915.4(GRHL2):c.21-2A>G AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Oct 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001782234.4
Allele description [Variation Report for NM_024915.4(GRHL2):c.21-2A>G]
NM_024915.4(GRHL2):c.21-2A>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Neurodevelopmental disorder with movement abnormalities, abnormal gait, and auti...
Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic featuresMedGen
-
Intestinal malrotation
Intestinal malrotationMedGen
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Mar 16, 2024