Variant (rsID / SNP)

rs59175042

rs59175042 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT10. Location: chromosome 17, position 38,978,366. Clinical significance in the table: Pathogenic.

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Reference-table entries

KRT10Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:38978366
Cytoband: 17q21.2
HGVS: NM_000421.5(KRT10):c.472G>C (p.Ala158Pro)
Allele change: Missense_A158P

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.