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Variant (rsID / SNP)

rs36007437

CCDC110

rs36007437 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC110. Location: chromosome 4, position 186,380,295. The table records no clinical significance for this variant.

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Reference-table entries

CCDC110Not classified
Variant type
synonymous_variant
Chromosome / position
4:186380295
HGVS
NM_152775.4,c.1446T>C,p.Asn482Asn
Allele change
Synonymous_N482N

Public references

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