Variant (rsID / SNP)

rs2280637

rs2280637 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PREX2. Location: chromosome 8, position 69,143,589. The table records no clinical significance for this variant.

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Reference-table entries

PREX2Not classified

Variant type: synonymous_variant
Chromosome / position: 8:69143589
HGVS: NM_024870.4,c.4797A>G,p.Pro1599Pro
Allele change: Synonymous_P1599P

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.