Variant (rsID / SNP)
rs2239822
rs2239822 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYTH4. Location: chromosome 22, position 37,699,377. The table records no clinical significance for this variant.
Reference-table entries
CYTH4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 22:37699377
- HGVS
- NM_013385.5,c.630T>C,p.Phe210Phe
- Allele change
- Synonymous_F153F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.