Variant (rsID / SNP)

rs369107336

rs369107336 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WFS1. Location: chromosome 4, position 6,303,891. Clinical significance in the table: Likely benign.

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Reference-table entries

WFS1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:6303891
Cytoband: 4p16.1
HGVS: NM_006005.3(WFS1):c.2369C>G (p.Ser790Trp)
Allele change: Missense_S790W

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.