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Variant (rsID / SNP)

rs8182306

KRT13

rs8182306 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT13. Location: chromosome 17, position 39,661,689. The table records no clinical significance for this variant.

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Reference-table entries

KRT13Not classified
Variant type
synonymous_variant
Chromosome / position
17:39661689
HGVS
NM_153490.3,c.114C>T,p.Ser38Ser
Allele change
Synonymous_S38S

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.