GRCh37/hg19 17q21.31(chr17:44121342-44368212)x3 AND not provided
Clinical significance:Benign (Last evaluated: Mar 14, 2014)
Review status:
- Based on:
- 1 submission [Details]
- Record status:
- current
- Accession:
- RCV000739534.1
Allele description [Variation Report for GRCh37/hg19 17q21.31(chr17:44121342-44368212)x3]
GRCh37/hg19 17q21.31(chr17:44121342-44368212)x3
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 23, 2022