Variant (rsID / SNP)

rs4310250

rs4310250 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRRC2B. Location: chromosome 9, position 134,346,315. The table records no clinical significance for this variant.

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Reference-table entries

PRRC2BNot classified

Variant type: synonymous_variant
Chromosome / position: 9:134346315
HGVS: NM_001384818.1,c.2052T>C,p.Arg684Arg
Allele change: Synonymous_R684R

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.