Variant (rsID / SNP)

rs3796375

rs3796375 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FYCO1. Location: chromosome 3, position 46,008,790. Clinical significance in the table: Benign.

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Reference-table entries

FYCO1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:46008790
Cytoband: 3p21.31
HGVS: NM_024513.4(FYCO1):c.2036C>T (p.Ala679Val)
Allele change: Missense_A679V

Associated conditions / phenotypes

Cataract 18

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.