Variant (rsID / SNP)
rs4658360
rs4658360 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GBP6. Location: chromosome 1, position 89,847,411. The table records no clinical significance for this variant.
Reference-table entries
GBP6Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:89847411
- HGVS
- NM_198460.3,c.1030C>T,p.Leu344Phe
- Allele change
- Missense_L344F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.