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Variant (rsID / SNP)

rs35031397

WFS1

rs35031397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WFS1. Location: chromosome 4, position 6,302,816. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

WFS1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
4:6302816
Cytoband
4p16.1
HGVS
NM_006005.3(WFS1):c.1294C>G (p.Leu432Val)
Allele change
Missense_L432V

Associated conditions / phenotypes

WFS1-Related Spectrum Disorders|Monogenic diabetes|Wolfram syndrome 1|Autosomal dominant nonsyndromic hearing loss 6

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.