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Variant (rsID / SNP)

rs6046790

CFAP61

rs6046790 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFAP61. Location: chromosome 20, position 20,303,376. The table records no clinical significance for this variant.

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Reference-table entries

CFAP61Not classified
Variant type
intron_variant
Chromosome / position
20:20303376
HGVS
NM_015585.4,c.3423-19099G>A
Allele change
Silent

Public references

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