Variant (rsID / SNP)

rs2224391

rs2224391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LYRM4, FARS2. Location: chromosome 6, position 5,260,936. Clinical significance in the table: Benign.

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Reference-table entries

LYRM4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:5260936
Cytoband: 6p25.1
HGVS: NM_020408.6(LYRM4):c.31T>G (p.Ser11Ala)
Allele change: Silent

Associated conditions / phenotypes

Combined oxidative phosphorylation deficiency 19

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.