Variant (rsID / SNP)

rs58058996

rs58058996 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT5. Location: chromosome 12, position 52,913,599. Clinical significance in the table: Pathogenic.

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Reference-table entries

KRT5Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 12:52913599
Cytoband: 12q13.13
HGVS: NM_000424.4(KRT5):c.482T>G (p.Ile161Ser)
Allele change: Missense_I161S

Associated conditions / phenotypes

Epidermolysis bullosa simplex 2C, localized|Epidermolysis bullosa simplex 1C, localized

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.