Variant (rsID / SNP)
rs4846382
rs4846382 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HHIPL2. Location: chromosome 1, position 222,721,288. The table records no clinical significance for this variant.
Reference-table entries
HHIPL2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:222721288
- HGVS
- NM_024746.4,c.99G>A,p.Leu33Leu
- Allele change
- Synonymous_L33L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.