Variant (rsID / SNP)
rs7568529
rs7568529 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRF3. Location: chromosome 2, position 26,534,801. The table records no clinical significance for this variant.
Reference-table entries
ADGRF3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:26534801
- HGVS
- NM_001145168.1,c.1795C>T,p.His599Tyr
- Allele change
- Missense_H400Y
Associated conditions / phenotypes
Missense_H599Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.