Variant (rsID / SNP)

rs11525060

rs11525060 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF425. Location: chromosome 7, position 148,801,091. The table records no clinical significance for this variant.

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Reference-table entries

ZNF425Not classified

Variant type: synonymous_variant
Chromosome / position: 7:148801091
HGVS: NM_001001661.3,c.1872C>T,p.Asn624Asn
Allele change: Synonymous_N624N

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.