Variant (rsID / SNP)

rs34252679

rs34252679 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRRC1. Location: chromosome 5, position 126,865,997. The table records no clinical significance for this variant.

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Reference-table entries

PRRC1Not classified

Variant type: synonymous_variant
Chromosome / position: 5:126865997
HGVS: NM_001286808.2,c.666G>A,p.Gly222Gly
Allele change: Synonymous_G222G

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.