Variant (rsID / SNP)
rs342706
rs342706 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPC5. Location: chromosome 13, position 92,417,058. The table records no clinical significance for this variant.
Reference-table entries
GPC5Not classified
- Variant type
- intron_variant
- Chromosome / position
- 13:92417058
- HGVS
- NM_004466.6,c.1280+8384T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.