Variant (rsID / SNP)

rs77919366

rs77919366 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT10. Location: chromosome 17, position 38,978,462. Clinical significance in the table: Benign.

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Reference-table entries

KRT10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:38978462
Cytoband: 17q21.2
HGVS: NM_000421.5(KRT10):c.376G>A (p.Gly126Ser)
Allele change: Missense_G126S

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.