Variant (rsID / SNP)

rs148941150

rs148941150 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLG2. Location: chromosome 17, position 62,488,876. Clinical significance in the table: Uncertain significance.

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Reference-table entries

POLG2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 17:62488876
Cytoband: 17q23.3
HGVS: NM_007215.4(POLG2):c.703A>G (p.Thr235Ala)
Allele change: Missense_T235A

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.