Variant (rsID / SNP)

rs10876354

rs10876354 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT79. Location: chromosome 12, position 53,217,701. The table records no clinical significance for this variant.

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Reference-table entries

KRT79Not classified

Variant type: synonymous_variant
Chromosome / position: 12:53217701
HGVS: NM_175834.3,c.1116G>T,p.Leu372Leu
Allele change: Synonymous_L372L

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.