Variant (rsID / SNP)

rs3733576

rs3733576 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAP3. Location: chromosome 4, position 17,586,703. The table records no clinical significance for this variant.

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Reference-table entries

LAP3Not classified

Variant type: synonymous_variant
Chromosome / position: 4:17586703
HGVS: NM_015907.3,c.648T>C,p.Ala216Ala
Allele change: Synonymous_A216A

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.