Variant (rsID / SNP)

rs151006368

rs151006368 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RRN3, PDXDC1. Location: chromosome 16, position 15,185,186. Clinical significance in the table: Benign.

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Reference-table entries

RRN3Benign

Clinical significance (as recorded): Benign
Variant type: missense_variant
Chromosome / position: 16:15185186
HGVS: NM_018427.5,c.238G>A,p.Asp80Asn
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.