Variant (rsID / SNP)

rs2571174

rs2571174 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF229. Location: chromosome 19, position 44,934,489. The table records no clinical significance for this variant.

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Reference-table entries

ZNF229Not classified

Variant type: missense_variant
Chromosome / position: 19:44934489
HGVS: NM_014518.4,c.467C>T,p.Ser156Phe
Allele change: Missense_S156F

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.