Variant (rsID / SNP)
rs7139733
rs7139733 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRYL1. Location: chromosome 13, position 21,086,599. The table records no clinical significance for this variant.
Reference-table entries
CRYL1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 13:21086599
- HGVS
- NM_015974.3,c.132C>T,p.Asn44Asn
- Allele change
- Synonymous_N44N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.