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Variant (rsID / SNP)

rs1475865

ABHD16A

rs1475865 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABHD16A. Location: chromosome 6, position 31,657,413. The table records no clinical significance for this variant.

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Reference-table entries

ABHD16ANot classified
Variant type
synonymous_variant
Chromosome / position
6:31657413
HGVS
NM_021160.3,c.1026A>G,p.Leu342Leu
Allele change
Silent

Public references

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