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Variant (rsID / SNP)

rs10865456

MAPRE3

rs10865456 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAPRE3. Location: chromosome 2, position 27,246,285. The table records no clinical significance for this variant.

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Reference-table entries

MAPRE3Not classified
Variant type
synonymous_variant
Chromosome / position
2:27246285
HGVS
NM_001303050.2,c.207C>T,p.His69His
Allele change
Synonymous_H69H

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.