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Variant (rsID / SNP)

rs1042858

RRM1

rs1042858 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RRM1. Location: chromosome 11, position 4,159,466. The table records no clinical significance for this variant.

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Reference-table entries

RRM1Not classified
Variant type
synonymous_variant
Chromosome / position
11:4159466
HGVS
NM_001033.5,c.2232G>A,p.Ala744Ala
Allele change
Synonymous_A744A

Associated conditions / phenotypes

Lung Cancer

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.