Variant (rsID / SNP)

rs9891361

rs9891361 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT13. Location: chromosome 17, position 39,659,913. Clinical significance in the table: Benign.

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Reference-table entries

KRT13Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:39659913
Cytoband: 17q21.2
HGVS: NM_153490.3(KRT13):c.560C>T (p.Ala187Val)
Allele change: Missense_A187V

Associated conditions / phenotypes

White sponge nevus 2

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.