Variant (rsID / SNP)
rs3762001
rs3762001 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FUCA2. Location: chromosome 6, position 143,823,112. The table records no clinical significance for this variant.
Reference-table entries
FUCA2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:143823112
- HGVS
- NM_032020.5,c.1111C>T,p.His371Tyr
- Allele change
- Missense_H371Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
