Variant (rsID / SNP)
rs3861878
rs3861878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMX1B. Location: chromosome 9, position 129,461,912. Clinical significance in the table: Benign.
Reference-table entries
LMX1BBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:129461912
- Cytoband
- 9q33.3
- HGVS
- NM_001174147.2(LMX1B):c.*3182A>G
- Allele change
- Silent
Associated conditions / phenotypes
Nail-patella syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.