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Variant (rsID / SNP)

rs3130071

PRRC2A

rs3130071 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRRC2A. Location: chromosome 6, position 31,594,628. The table records no clinical significance for this variant.

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Reference-table entries

PRRC2ANot classified
Variant type
synonymous_variant
Chromosome / position
6:31594628
HGVS
NM_004638.4,c.1062T>A,p.Gly354Gly
Allele change
Synonymous_G354G

Public references

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