Variant (rsID / SNP)
rs146931391
rs146931391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMBR1. Location: chromosome 7, position 156,474,707. Clinical significance in the table: Benign.
Reference-table entries
LMBR1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:156474707
- Cytoband
- 7q36.3
- HGVS
- NM_022458.4(LMBR1):c.*2065A>G
- Allele change
- Silent
Associated conditions / phenotypes
Polydactyly of a triphalangeal thumb
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.