Variant (rsID / SNP)
rs1427329
rs1427329 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MARCHF7. Location: chromosome 2, position 160,604,812. The table records no clinical significance for this variant.
Reference-table entries
MARCHF7Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:160604812
- HGVS
- NM_001282805.2,c.1011C>T,p.Pro337Pro
- Allele change
- Synonymous_P281P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
