Variant (rsID / SNP)

rs1553960

rs1553960 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAPOLB, RADIL. Location: chromosome 7, position 4,900,095. The table records no clinical significance for this variant.

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Reference-table entries

PAPOLBNot classified

Variant type: synonymous_variant
Chromosome / position: 7:4900095
HGVS: NM_020144.5,c.1347T>C,p.Asn449Asn
Allele change: Silent

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.