NM_017662.5(TRPM6):c.1985C>T (p.Ser662Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003186534.2
Allele description [Variation Report for NM_017662.5(TRPM6):c.1985C>T (p.Ser662Leu)]
NM_017662.5(TRPM6):c.1985C>T (p.Ser662Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Appetite
AppetiteNatural recurring desire for food. Alterations may be induced by APPETITE DEPRESSANTS or APPETITE STIMULANTS.<br/>MeSH
-
D001066 (1)
MeSH
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024