GRCh37/hg19 8q12.3(chr8:63122839-64926318) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002053767.3
Allele description [Variation Report for GRCh37/hg19 8q12.3(chr8:63122839-64926318)]
GRCh37/hg19 8q12.3(chr8:63122839-64926318)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Glycine N-methyltransferase deficiency
Glycine N-methyltransferase deficiencyMedGen
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Mar 26, 2023