Variant (rsID / SNP)

rs2604953

rs2604953 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT32. Location: chromosome 17, position 39,616,430. The table records no clinical significance for this variant.

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Reference-table entries

KRT32Not classified

Variant type: missense_variant
Chromosome / position: 17:39616430
HGVS: NM_002278.3,c.1279C>A,p.Pro427Thr
Allele change: Missense_P427T

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.