Variant (rsID / SNP)

rs77148611

rs77148611 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF407. Location: chromosome 18, position 72,344,052. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZNF407Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:72344052
Cytoband: 18q22.3
HGVS: NM_017757.3(ZNF407):c.1077A>G (p.Val359=)
Allele change: Synonymous_V359V

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.