Variant (rsID / SNP)

rs2277809

rs2277809 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFAP410. Location: chromosome 21, position 45,751,822. Clinical significance in the table: Benign.

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Reference-table entries

CFAP410Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 21:45751822
Cytoband: 21q22.3
HGVS: NM_004928.3(CFAP410):c.449C>T (p.Thr150Ile)
Allele change: Missense_T150I

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.