Variant (rsID / SNP)

rs2298815

rs2298815 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKRD13D. Location: chromosome 11, position 67,068,859. The table records no clinical significance for this variant.

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Reference-table entries

ANKRD13DNot classified

Variant type: synonymous_variant
Chromosome / position: 11:67068859
HGVS: NM_207354.3,c.1338T>C,p.Val446Val
Allele change: Synonymous_V446V

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.