Variant (rsID / SNP)
rs3814205
rs3814205 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCSER2. Location: chromosome 10, position 86,131,059. The table records no clinical significance for this variant.
Reference-table entries
CCSER2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:86131059
- HGVS
- NM_001284240.2,c.251A>G,p.Asn84Ser
- Allele change
- Missense_N84S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.