Variant (rsID / SNP)

rs1054428

rs1054428 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANXA2R. Location: chromosome 5, position 43,039,793. The table records no clinical significance for this variant.

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Reference-table entries

ANXA2RNot classified

Variant type: missense_variant
Chromosome / position: 5:43039793
HGVS: NM_001014279.3,c.356A>G,p.Gln119Arg
Allele change: Silent

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.