Variant (rsID / SNP)
rs7940667
rs7940667 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NECTIN1. Location: chromosome 11, position 119,510,644. Clinical significance in the table: Benign.
Reference-table entries
NECTIN1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- missense_variant
- Chromosome / position
- 11:119510644
- HGVS
- NM_203285.2,c.1082T>G,p.Val361Gly
- Allele change
- Missense_V361G
Associated conditions / phenotypes
Cleft Lip/palate-Ectodermal Dysplasia Syndrome|Cleft Lip
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.