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Variant (rsID / SNP)

rs17843021

KRT39

rs17843021 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT39. Location: chromosome 17, position 39,116,728. The table records no clinical significance for this variant.

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Reference-table entries

KRT39Not classified
Variant type
missense_variant
Chromosome / position
17:39116728
HGVS
NM_213656.4,c.1022C>T,p.Thr341Met
Allele change
Missense_T341M

Public references

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