Variant (rsID / SNP)
rs4808907
rs4808907 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SUGP2. Location: chromosome 19, position 19,136,541. The table records no clinical significance for this variant.
Reference-table entries
SUGP2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:19136541
- HGVS
- NM_001321698.1,c.658G>A,p.Gly220Ser
- Allele change
- Missense_G220S
Associated conditions / phenotypes
Missense_G206S|Missense_G220S|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.