Variant (rsID / SNP)

rs8064733

rs8064733 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT40. Location: chromosome 17, position 39,135,084. The table records no clinical significance for this variant.

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Reference-table entries

KRT40Not classified

Variant type: missense_variant
Chromosome / position: 17:39135084
HGVS: NM_001385217.1,c.1168T>C,p.Trp390Arg
Allele change: Missense_W390R

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.