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Variant (rsID / SNP)

rs2767434

CFAP46

rs2767434 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFAP46. Location: chromosome 10, position 134,622,408. The table records no clinical significance for this variant.

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Reference-table entries

CFAP46Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
10:134622408
HGVS
NM_001200049.3,c.7665A>G,p.Arg2555Arg
Allele change
Synonymous_R2555R

Public references

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