Variant (rsID / SNP)

rs3770214

rs3770214 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF142. Location: chromosome 2, position 219,508,988. The table records no clinical significance for this variant.

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Reference-table entries

ZNF142Not classified

Variant type: missense_variant
Chromosome / position: 2:219508988
HGVS: NM_001366290.3,c.2851A>G,p.Ser951Gly
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.