Variant (rsID / SNP)
rs17157825
rs17157825 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MARCHF8. Location: chromosome 10, position 45,958,676. The table records no clinical significance for this variant.
Reference-table entries
MARCHF8Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:45958676
- HGVS
- NM_001282866.2,c.1011C>T,p.Ser337Ser
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.