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Variant (rsID / SNP)

rs4832524

KCNS3

rs4832524 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNS3. Location: chromosome 2, position 18,113,623. The table records no clinical significance for this variant.

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Reference-table entries

KCNS3Not classified
Variant type
missense_variant
Chromosome / position
2:18113623
HGVS
NM_001282428.2,c.1348A>G,p.Thr450Ala
Allele change
Missense_T450A

Public references

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