Variant (rsID / SNP)

rs1805069

rs1805069 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WFS1. Location: chromosome 4, position 6,303,248. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

WFS1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:6303248
Cytoband: 4p16.1
HGVS: NM_006005.3(WFS1):c.1726G>A (p.Gly576Ser)
Allele change: Missense_G576S

Associated conditions / phenotypes

Autosomal dominant nonsyndromic hearing loss 6|WFS1-Related Spectrum Disorders|Monogenic diabetes

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.