Variant (rsID / SNP)
rs3735400
rs3735400 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANLN. Location: chromosome 7, position 36,438,709. The table records no clinical significance for this variant.
Reference-table entries
ANLNNot classified
- Variant type
- missense_variant
- Chromosome / position
- 7:36438709
- HGVS
- NM_018685.5,c.194C>G,p.Ser65Trp
- Allele change
- Missense_S65W
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.