Variant (rsID / SNP)

rs3820011

rs3820011 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFAP74. Location: chromosome 1, position 1,888,193. The table records no clinical significance for this variant.

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Reference-table entries

CFAP74Not classified

Variant type: missense_variant
Chromosome / position: 1:1888193
HGVS: NM_001304360.2,c.1882G>T,p.Gly628Cys
Allele change: Missense_G628C

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.