Variant (rsID / SNP)
rs113346639
rs113346639 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LPIN2. Location: chromosome 18, position 2,918,789. Clinical significance in the table: Benign.
Reference-table entries
LPIN2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 18:2918789
- Cytoband
- 18p11.31
- HGVS
- NM_001375808.2(LPIN2):c.*1502G>A
- Allele change
- Silent
Associated conditions / phenotypes
Majeed syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.