Variant (rsID / SNP)
rs3764021
rs3764021 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLEC2D. Location: chromosome 12, position 9,833,628. The table records no clinical significance for this variant.
Reference-table entries
CLEC2DNot classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 12:9833628
- HGVS
- NM_001004419.5,c.171C>T,p.Ser57Ser
- Allele change
- Silent
Associated conditions / phenotypes
Inflammatory Bowel Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.