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Variant (rsID / SNP)

rs3734619

KCNK16

rs3734619 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNK16. Location: chromosome 6, position 39,290,200. The table records no clinical significance for this variant.

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Reference-table entries

KCNK16Not classified
Variant type
synonymous_variant
Chromosome / position
6:39290200
HGVS
NM_001135105.2,c.117G>A,p.Ala39Ala
Allele change
Silent

Public references

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