Variant (rsID / SNP)
rs1156287
rs1156287 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STXBP4. Location: chromosome 17, position 53,076,799. The table records no clinical significance for this variant.
Reference-table entries
STXBP4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:53076799
- HGVS
- NM_001398481.1,c.274G>A,p.Gly92Arg
- Allele change
- Missense_G92R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.