Variant (rsID / SNP)

rs9921361

rs9921361 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF778. Location: chromosome 16, position 89,294,439. The table records no clinical significance for this variant.

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Reference-table entries

ZNF778Not classified

Variant type: missense_variant
Chromosome / position: 16:89294439
HGVS: NM_001201407.2,c.1743G>T,p.Gln581His
Allele change: Silent

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.