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Variant (rsID / SNP)

rs2723089

CEP68

rs2723089 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP68. Location: chromosome 2, position 65,299,300. The table records no clinical significance for this variant.

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Reference-table entries

CEP68Not classified
Variant type
missense_variant
Chromosome / position
2:65299300
HGVS
NM_001319100.2,c.1070G>C,p.Cys357Ser
Allele change
Missense_C357S

Public references

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