Variant (rsID / SNP)

rs1469602

rs1469602 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZC3H14. Location: chromosome 14, position 89,042,180. Clinical significance in the table: Likely benign.

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Reference-table entries

ZC3H14Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:89042180
Cytoband: 14q31.3
HGVS: NM_024824.5(ZC3H14):c.1023-4T>G
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.