GRCh38/hg38 15q11.2-13.1(chr15:23375044-28300209)x1 AND See cases
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Jun 22, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000139986.6
Allele description [Variation Report for GRCh38/hg38 15q11.2-13.1(chr15:23375044-28300209)x1]
GRCh38/hg38 15q11.2-13.1(chr15:23375044-28300209)x1
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
-
SNORD116-13 small nucleolar RNA, C/D box 116-13 [Homo sapiens]
SNORD116-13 small nucleolar RNA, C/D box 116-13 [Homo sapiens]Gene ID:100033425Gene
-
LOC130056716 [Homo sapiens]
LOC130056716 [Homo sapiens]Gene ID:130056716Gene
-
LOC129390675 [Homo sapiens]
LOC129390675 [Homo sapiens]Gene ID:129390675Gene
-
SNORD116-15 small nucleolar RNA, C/D box 116-15 [Homo sapiens]
SNORD116-15 small nucleolar RNA, C/D box 116-15 [Homo sapiens]Gene ID:100033427Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 7, 2024