Variant (rsID / SNP)
rs5997917
rs5997917 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LIMK2. Location: chromosome 22, position 31,621,792. The table records no clinical significance for this variant.
Reference-table entries
LIMK2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 22:31621792
- HGVS
- NM_005569.4,c.103G>A,p.Gly35Ser
- Allele change
- Missense_G35S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.