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Variant (rsID / SNP)

rs494791

CCDC90B

rs494791 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC90B. Location: chromosome 11, position 82,996,986. The table records no clinical significance for this variant.

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Reference-table entries

CCDC90BNot classified
Variant type
missense_variant
Chromosome / position
11:82996986
HGVS
NM_021825.5,c.30T>G,p.Phe10Leu
Allele change
Missense_F10L

Public references

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