Variant (rsID / SNP)
rs1010425
rs1010425 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIGLEC10. Location: chromosome 19, position 51,920,613. The table records no clinical significance for this variant.
Reference-table entries
SIGLEC10Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:51920613
- HGVS
- NM_033130.5,c.144G>A,p.Gln48Gln
- Allele change
- Synonymous_Q48Q
Associated conditions / phenotypes
Synonymous_Q48Q|Synonymous_Q48Q|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.