Variant (rsID / SNP)

rs4260880

rs4260880 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PREX2. Location: chromosome 8, position 69,020,496. The table records no clinical significance for this variant.

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Reference-table entries

PREX2Not classified

Variant type: synonymous_variant
Chromosome / position: 8:69020496
HGVS: NM_024870.4,c.2868T>C,p.Ser956Ser
Allele change: Synonymous_S956S

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.