Variant (rsID / SNP)

rs574976629

rs574976629 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIX1. Location: chromosome 14, position 61,112,234. Clinical significance in the table: Likely benign.

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Reference-table entries

SIX1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:61112234
Cytoband: 14q23.1
HGVS: NM_005982.4(SIX1):c.*767A>T
Allele change: Silent

Associated conditions / phenotypes

Autosomal dominant nonsyndromic hearing loss 23|Branchiootic syndrome 3

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.