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Variant (rsID / SNP)

rs11101618

KNDC1

rs11101618 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KNDC1. Location: chromosome 10, position 134,996,869. The table records no clinical significance for this variant.

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Reference-table entries

KNDC1Not classified
Variant type
missense_variant
Chromosome / position
10:134996869
HGVS
NM_152643.8,c.382G>T,p.Ala128Ser
Allele change
Missense_A128S

Public references

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