Variant (rsID / SNP)

rs267606804

rs267606804 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FECH. Location: chromosome 18, position 55,217,991. Clinical significance in the table: no interpretation for the single variant.

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Reference-table entries

FECHOther

Clinical significance (as recorded): no interpretation for the single variant
Variant type: single nucleotide variant
Chromosome / position: 18:55217991
Cytoband: 18q21.31
HGVS: NM_000140.5(FECH):c.1225C>T (p.Pro409Ser)
Allele change: Missense_P415S

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.