Variant (rsID / SNP)

rs75994611

rs75994611 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF407. Location: chromosome 18, position 72,343,156. Clinical significance in the table: Benign.

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Reference-table entries

ZNF407Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:72343156
Cytoband: 18q22.3
HGVS: NM_017757.3(ZNF407):c.181A>G (p.Ser61Gly)
Allele change: Missense_S61G

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.