Variant (rsID / SNP)

rs267607131

rs267607131 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TOP1. Location: chromosome 20, position 39,742,755. Clinical significance in the table: no interpretation for the single variant.

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Reference-table entries

TOP1Other

Clinical significance (as recorded): no interpretation for the single variant
Variant type: single nucleotide variant
Chromosome / position: 20:39742755
Cytoband: 20q12
HGVS: NM_003286.4(TOP1):c.1598A>G (p.Asp533Gly)
Allele change: Missense_D533G

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.