Variant (rsID / SNP)

rs2125579

rs2125579 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF235. Location: chromosome 19, position 44,792,701. The table records no clinical significance for this variant.

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Reference-table entries

ZNF235Not classified

Variant type: missense_variant
Chromosome / position: 19:44792701
HGVS: NM_004234.4,c.887A>C,p.His296Pro
Allele change: Missense_H296P

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.