Variant (rsID / SNP)
rs2236369
rs2236369 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NCR2. Location: chromosome 6, position 41,309,552. The table records no clinical significance for this variant.
Reference-table entries
NCR2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:41309552
- HGVS
- NM_004828.4,c.415T>C,p.Ser139Pro
- Allele change
- Missense_S139P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.