Variant (rsID / SNP)

rs1381057

rs1381057 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLQ. Location: chromosome 3, position 121,154,974. The table records no clinical significance for this variant.

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Reference-table entries

POLQNot classified

Variant type: missense_variant
Chromosome / position: 3:121154974
HGVS: NM_199420.4,c.7538A>G,p.Gln2513Arg
Allele change: Missense_Q2513R

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.