Variant (rsID / SNP)

rs2272719

rs2272719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DEFA5. Location: chromosome 8, position 6,913,031. The table records no clinical significance for this variant.

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Reference-table entries

DEFA5Not classified

Variant type: synonymous_variant
Chromosome / position: 8:6913031
HGVS: NM_021010.3,c.207C>T,p.Thr69Thr
Allele change: Synonymous_T69T

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.