Variant (rsID / SNP)

rs12833456

rs12833456 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT72. Location: chromosome 12, position 52,986,187. The table records no clinical significance for this variant.

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Reference-table entries

KRT72Not classified

Variant type: missense_variant
Chromosome / position: 12:52986187
HGVS: NM_001146225.2,c.791A>G,p.Tyr264Cys
Allele change: Missense_Y264C

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.