Variant (rsID / SNP)

rs894039

rs894039 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLBA1. Location: chromosome 14, position 105,461,067. The table records no clinical significance for this variant.

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Reference-table entries

CLBA1Not classified

Variant type: synonymous_variant
Chromosome / position: 14:105461067
HGVS: NM_174891.4,c.949C>T,p.Leu317Leu
Allele change: Synonymous_L317L

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.