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Variant (rsID / SNP)

rs2276598

DNMT3A

rs2276598 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNMT3A. Location: chromosome 2, position 25,469,502. The table records no clinical significance for this variant.

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Reference-table entries

DNMT3ANot classified
Variant type
synonymous_variant
Chromosome / position
2:25469502
HGVS
NM_022552.5,c.1266G>A,p.Leu422Leu
Allele change
Synonymous_L233L

Associated conditions / phenotypes

Transposition of the Great Arteries, Dextro-Looped

Public references

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