Variant (rsID / SNP)

rs314299

rs314299 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZAN. Location: chromosome 7, position 100,371,473. Clinical significance in the table: Benign.

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Reference-table entries

ZANBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:100371473
Cytoband: 7q22.1
HGVS: NM_003386.3(ZAN):c.5764C>T (p.His1922Tyr)
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.