Variant (rsID / SNP)

rs104893882

rs104893882 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WFS1. Location: chromosome 4, position 6,303,423. Clinical significance in the table: Pathogenic.

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Reference-table entries

WFS1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 4:6303423
Cytoband: 4p16.1
HGVS: NM_006005.3(WFS1):c.1901A>C (p.Lys634Thr)
Allele change: Missense_K634T

Associated conditions / phenotypes

Autosomal dominant nonsyndromic hearing loss 6

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.