Variant (rsID / SNP)

rs1062708

rs1062708 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RUVBL2. Location: chromosome 19, position 49,513,273. The table records no clinical significance for this variant.

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Reference-table entries

RUVBL2Not classified

Variant type: synonymous_variant
Chromosome / position: 19:49513273
HGVS: NM_006666.3,c.613C>T,p.Leu205Leu
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.