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Variant (rsID / SNP)

rs16885577

KCNU1

rs16885577 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNU1. Location: chromosome 8, position 36,788,479. The table records no clinical significance for this variant.

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Reference-table entries

KCNU1Not classified
Variant type
missense_variant
Chromosome / position
8:36788479
HGVS
NM_001031836.3,c.2747A>G,p.Asn916Ser
Allele change
Missense_N916S

Public references

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