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Variant (rsID / SNP)

rs41317288

KNDC1

rs41317288 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KNDC1. Location: chromosome 10, position 135,010,635. The table records no clinical significance for this variant.

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Reference-table entries

KNDC1Not classified
Variant type
missense_variant
Chromosome / position
10:135010635
HGVS
NM_152643.8,c.1808G>A,p.Cys603Tyr
Allele change
Missense_C603Y

Public references

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