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Variant (rsID / SNP)

rs17244028

CCDC34

rs17244028 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC34. Location: chromosome 11, position 27,362,359. The table records no clinical significance for this variant.

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Reference-table entries

CCDC34Not classified
Variant type
missense_variant
Chromosome / position
11:27362359
HGVS
NM_030771.2,c.791A>C,p.Glu264Ala
Allele change
Missense_E264A

Public references

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