Variant (rsID / SNP)

rs2273782

rs2273782 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RLN1. Location: chromosome 9, position 5,335,470. The table records no clinical significance for this variant.

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Reference-table entries

RLN1Not classified

Variant type: synonymous_variant
Chromosome / position: 9:5335470
HGVS: NM_006911.4,c.339G>A,p.Gln113Gln
Allele change: Synonymous_Q113Q

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.