Variant (rsID / SNP)

rs11084162

rs11084162 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF534. Location: chromosome 19, position 52,938,417. The table records no clinical significance for this variant.

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Reference-table entries

ZNF534Not classified

Variant type: missense_variant
Chromosome / position: 19:52938417
HGVS: NM_001143939.3,c.265A>G,p.Ile89Val
Allele change: Missense_I76V

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.