NM_002693.3(POLG):c.2165G>T (p.Arg722Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 10, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002426911.2
Allele description [Variation Report for NM_002693.3(POLG):c.2165G>T (p.Arg722Leu)]
NM_002693.3(POLG):c.2165G>T (p.Arg722Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
KIRREL3 [Phocoena sinus]
KIRREL3 [Phocoena sinus]Gene ID:116757488Gene
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Last Updated: Sep 29, 2024