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Variant (rsID / SNP)

rs3736403

CFAP65

rs3736403 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFAP65. Location: chromosome 2, position 219,905,247. The table records no clinical significance for this variant.

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Reference-table entries

CFAP65Not classified
Variant type
missense_variant
Chromosome / position
2:219905247
HGVS
NM_001278295.1,c.65A>G,p.Asn22Ser
Allele change
Silent

Public references

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