Variant (rsID / SNP)

rs887387

rs887387 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP2A3. Location: chromosome 17, position 3,828,702. The table records no clinical significance for this variant.

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Reference-table entries

ATP2A3Not classified

Variant type: synonymous_variant
Chromosome / position: 17:3828702
HGVS: NM_174955.3,c.3102A>G,p.Arg1034Arg
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.