Variant (rsID / SNP)

rs41264699

rs41264699 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WFS1. Location: chromosome 4, position 6,293,040. 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: 4:6293040
Cytoband: 4p16.1
HGVS: NM_006005.3(WFS1):c.577A>C (p.Lys193Gln)
Allele change: Missense_K193Q

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.