Variant (rsID / SNP)

rs12977303

rs12977303 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF404. Location: chromosome 19, position 44,377,669. The table records no clinical significance for this variant.

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Reference-table entries

ZNF404Not classified

Variant type: missense_variant
Chromosome / position: 19:44377669
HGVS: NM_001033719.3,c.697C>T,p.His233Tyr
Allele change: Missense_H230Y

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.