Variant (rsID / SNP)

rs6497671

rs6497671 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EARS2. Location: chromosome 16, position 23,536,684. Clinical significance in the table: Benign.

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Reference-table entries

EARS2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:23536684
Cytoband: 16p12.2
HGVS: NM_001083614.2(EARS2):c.1369A>G (p.Ser457Gly)
Allele change: Missense_S457G

Associated conditions / phenotypes

Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome

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.