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Variant (rsID / SNP)

rs16839032

NOP58

rs16839032 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOP58. Location: chromosome 2, position 203,157,538. The table records no clinical significance for this variant.

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Reference-table entries

NOP58Not classified
Variant type
synonymous_variant
Chromosome / position
2:203157538
HGVS
NM_015934.5,c.819A>G,p.Glu273Glu
Allele change
Synonymous_E273E

Public references

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