GRCh37/hg19 17q21.31(chr17:44164956-44292126)x3 AND not provided
Clinical significance:Benign (Last evaluated: Jul 25, 2016)
Review status:
- Based on:
- 1 submission [Details]
- Record status:
- current
- Accession:
- RCV000739558.2
Allele description [Variation Report for GRCh37/hg19 17q21.31(chr17:44164956-44292126)x3]
GRCh37/hg19 17q21.31(chr17:44164956-44292126)x3
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Mar 4, 2023