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Variant (rsID / SNP)

rs2269911

CLDN6

rs2269911 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLDN6. Location: chromosome 16, position 3,065,924. The table records no clinical significance for this variant.

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Reference-table entries

CLDN6Not classified
Variant type
synonymous_variant
Chromosome / position
16:3065924
HGVS
NM_021195.5,c.99C>T,p.Thr33Thr
Allele change
Synonymous_T33T

Public references

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