Variant (rsID / SNP)

rs45518831

rs45518831 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZC3H14. Location: chromosome 14, position 89,063,102. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ZC3H14Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:89063102
Cytoband: 14q31.3
HGVS: NM_024824.5(ZC3H14):c.1304C>T (p.Ser435Phe)
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.