Variant (rsID / SNP)
rs267607167
rs267607167 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VANGL2. Location: chromosome 1, position 160,390,961. Clinical significance in the table: risk factor.
Reference-table entries
VANGL2Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:160390961
- Cytoband
- 1q23.2
- HGVS
- NM_020335.3(VANGL2):c.1057C>T (p.Arg353Cys)
- Allele change
- Missense_R353C
Associated conditions / phenotypes
Neural tube defects, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.