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Variant (rsID / SNP)

rs2289603

RNF157

rs2289603 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF157. Location: chromosome 17, position 74,163,821. The table records no clinical significance for this variant.

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Reference-table entries

RNF157Not classified
Variant type
synonymous_variant
Chromosome / position
17:74163821
HGVS
NM_052916.3,c.354C>T,p.Tyr118Tyr
Allele change
Synonymous_Y118Y

Public references

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