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Variant (rsID / SNP)

rs807459

CLTCL1

rs807459 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLTCL1. Location: chromosome 22, position 19,223,352. The table records no clinical significance for this variant.

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Reference-table entries

CLTCL1Not classified
Variant type
missense_variant
Chromosome / position
22:19223352
HGVS
NM_007098.4,c.836A>G,p.Tyr279Cys
Allele change
Missense_Y279C

Public references

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