Variant (rsID / SNP)
rs74113801
rs74113801 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CELSR2. Location: chromosome 1, position 109,793,128. Clinical significance in the table: Benign.
Reference-table entries
CELSR2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- missense_variant
- Chromosome / position
- 1:109793128
- HGVS
- NM_001408.3,c.427C>T,p.Leu143Phe
- Allele change
- Missense_L143F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.