Variant (rsID / SNP)
rs2236359
rs2236359 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SNAP47. Location: chromosome 1, position 227,935,444. The table records no clinical significance for this variant.
Reference-table entries
SNAP47Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:227935444
- HGVS
- NM_001323935.1,c.142A>G,p.Arg48Gly
- Allele change
- Missense_R3G
Associated conditions / phenotypes
Missense_R48G|Missense_R48G|Missense_R3G|Silent|Missense_R3G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.