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Variant (rsID / SNP)

rs1545133

POLR1B

rs1545133 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLR1B. Location: chromosome 2, position 113,309,473. The table records no clinical significance for this variant.

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Reference-table entries

POLR1BNot classified
Variant type
missense_variant
Chromosome / position
2:113309473
HGVS
NM_001371969.1,c.884C>T,p.Ser295Leu
Allele change
Missense_S84L

Associated conditions / phenotypes

Missense_S295L|Missense_S333L

Public references

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