Variant (rsID / SNP)

rs6962772

rs6962772 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF789. Location: chromosome 7, position 99,081,730. The table records no clinical significance for this variant.

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Reference-table entries

ZNF789Not classified

Variant type: missense_variant
Chromosome / position: 7:99081730
HGVS: NM_213603.3,c.229A>G,p.Thr77Ala
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.