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Variant (rsID / SNP)

rs34399489

RNF213

rs34399489 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF213. Location: chromosome 17, position 78,313,562. The table records no clinical significance for this variant.

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Reference-table entries

RNF213Not classified
Variant type
synonymous_variant
Chromosome / position
17:78313562
HGVS
NM_001256071.3,c.5395C>T,p.Leu1799Leu
Allele change
Synonymous_L1799L

Public references

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