Variant (rsID / SNP)

rs2288958

rs2288958 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF57. Location: chromosome 19, position 2,917,287. The table records no clinical significance for this variant.

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Reference-table entries

ZNF57Not classified

Variant type: missense_variant
Chromosome / position: 19:2917287
HGVS: NM_173480.3,c.668C>A,p.Thr223Asn
Allele change: Missense_T223N

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.