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Variant (rsID / SNP)

rs17160348

CERS4

rs17160348 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CERS4. Location: chromosome 19, position 8,326,866. The table records no clinical significance for this variant.

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Reference-table entries

CERS4Not classified
Variant type
missense_variant
Chromosome / position
19:8326866
HGVS
NM_024552.3,c.1058C>T,p.Ala353Val
Allele change
Missense_A353V

Public references

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