Variant (rsID / SNP)

rs61749963

rs61749963 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COX20. Location: chromosome 1, position 245,006,474. Clinical significance in the table: Benign.

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Reference-table entries

COX20Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:245006474
Cytoband: 1q44
HGVS: NM_198076.6(COX20):c.353A>G (p.Asn118Ser)
Allele change: Missense_N118S

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.