Variant (rsID / SNP)

rs12781609

rs12781609 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFAP46. Location: chromosome 10, position 134,748,331. The table records no clinical significance for this variant.

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Reference-table entries

CFAP46Not classified

Variant type: missense_variant
Chromosome / position: 10:134748331
HGVS: NM_001200049.3,c.791G>A,p.Ser264Asn
Allele change: Missense_S264N

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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