Variant (rsID / SNP)

rs2269828

rs2269828 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AMIGO2, PCED1B. Location: chromosome 12, position 47,471,439. The table records no clinical significance for this variant.

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Reference-table entries

AMIGO2Not classified

Variant type: synonymous_variant
Chromosome / position: 12:47471439
HGVS: NM_001143668.1,c.1347C>T,p.Pro449Pro
Allele change: Synonymous_P449P

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.