Variant (rsID / SNP)

rs137955859

rs137955859 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FECH. Location: chromosome 18, position 55,214,815. Clinical significance in the table: Likely benign.

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Reference-table entries

FECHLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:55214815
Cytoband: 18q21.31
HGVS: NM_000140.5(FECH):c.*3129C>T
Allele change: Silent

Associated conditions / phenotypes

Protoporphyria, erythropoietic, 1

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.