Variant (rsID / SNP)

rs670741

rs670741 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT74. Location: chromosome 12, position 52,965,173. The table records no clinical significance for this variant.

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Reference-table entries

KRT74Not classified

Variant type: missense_variant
Chromosome / position: 12:52965173
HGVS: NM_175053.4,c.813A>C,p.Glu271Asp
Allele change: Missense_E271D

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.