Variant (rsID / SNP)

rs150936382

rs150936382 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WFS1. Location: chromosome 4, position 6,303,892. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

WFS1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:6303892
Cytoband: 4p16.1
HGVS: NM_006005.3(WFS1):c.2370G>A (p.Ser790=)
Allele change: Synonymous_S790S

Associated conditions / phenotypes

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

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.