Variant (rsID / SNP)

rs368587966

rs368587966 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLG. Location: chromosome 15, position 89,864,454. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

POLGConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 15:89864454
Cytoband: 15q26.1
HGVS: NM_002693.3(POLG):c.2636A>G (p.Gln879Arg)
Allele change: Missense_Q879R

Associated conditions / phenotypes

Progressive sclerosing poliodystrophy

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.