GRCh37/hg19 17q21.31(chr17:44275035-44277825)x4 AND not provided
Clinical significance:Benign (Last evaluated: Sep 23, 2014)
Review status:
- Based on:
- 1 submission [Details]
- Record status:
- current
- Accession:
- RCV000739604.1
Allele description [Variation Report for GRCh37/hg19 17q21.31(chr17:44275035-44277825)x4]
GRCh37/hg19 17q21.31(chr17:44275035-44277825)x4
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 23, 2022