Variant (rsID / SNP)

rs2478467

rs2478467 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLPSL2. Location: chromosome 6, position 35,745,655. The table records no clinical significance for this variant.

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Reference-table entries

CLPSL2Not classified

Variant type: missense_variant
Chromosome / position: 6:35745655
HGVS: NM_001286550.2,c.235C>T,p.Arg79Cys
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.