Variant (rsID / SNP)
rs34608563
rs34608563 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OLFML3. Location: chromosome 1, position 114,524,169. Clinical significance in the table: Benign.
Reference-table entries
OLFML3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- synonymous_variant
- Chromosome / position
- 1:114524169
- HGVS
- NM_020190.5,c.999C>T,p.Val333Val
- Allele change
- Synonymous_V333V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.