Variant (rsID / SNP)

rs871546

rs871546 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZBTB21. Location: chromosome 21, position 43,413,553. The table records no clinical significance for this variant.

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Reference-table entries

ZBTB21Not classified

Variant type: missense_variant
Chromosome / position: 21:43413553
HGVS: NM_001098402.2,c.652A>C,p.Lys218Gln
Allele change: Missense_K218Q

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.