Variant (rsID / SNP)

rs3794942

rs3794942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF407. Location: chromosome 18, position 72,343,181. Clinical significance in the table: Likely benign.

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Reference-table entries

ZNF407Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:72343181
Cytoband: 18q22.3
HGVS: NM_017757.3(ZNF407):c.206A>G (p.Asn69Ser)
Allele change: Missense_N69S

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.