Variant (rsID / SNP)
rs1168308
rs1168308 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRIP1. Location: chromosome 12, position 66,742,183. Clinical significance in the table: Benign.
Reference-table entries
GRIP1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:66742183
- Cytoband
- 12q14.3
- HGVS
- NM_001366722.1(GRIP1):c.*616T>C
- Allele change
- Silent
Associated conditions / phenotypes
Fraser syndrome 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.