Variant (rsID / SNP)
rs34467190
rs34467190 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLSCR4. Location: chromosome 3, position 145,913,061. The table records no clinical significance for this variant.
Reference-table entries
PLSCR4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:145913061
- HGVS
- NM_001128304.2,c.795C>A,p.Ser265Ser
- Allele change
- Synonymous_S265S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.