Variant (rsID / SNP)

rs141476300

rs141476300 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FYCO1. Location: chromosome 3, position 46,021,220. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

FYCO1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 3:46021220
Cytoband: 3p21.31
HGVS: NM_024513.4(FYCO1):c.265C>T (p.Arg89Cys)
Allele change: Missense_R89C

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.