Variant (rsID / SNP)
rs998147
rs998147 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYNE1. Location: chromosome 6, position 152,489,294. The table records no clinical significance for this variant.
Reference-table entries
SYNE1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:152489294
- HGVS
- NM_001347702.2,c.46A>G,p.Ser16Gly
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.