NM_001999.4(FBN2):c.4222+10C>A AND Ehlers-Danlos syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 1, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002279553.3
Allele description [Variation Report for NM_001999.4(FBN2):c.4222+10C>A]
NM_001999.4(FBN2):c.4222+10C>A
Condition(s)
-
PREDICTED: Homo sapiens odd-skipped related transcription factor 1 (OSR1), trans...
PREDICTED: Homo sapiens odd-skipped related transcription factor 1 (OSR1), transcript variant X2, misc_RNAgi|2217325594|ref|XR_007069636.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024