Variant (rsID / SNP)

rs6580870

rs6580870 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT7. Location: chromosome 12, position 52,631,313. The table records no clinical significance for this variant.

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Reference-table entries

KRT7Not classified

Variant type: missense_variant
Chromosome / position: 12:52631313
HGVS: NM_005556.4,c.557A>G,p.His186Arg
Allele change: Missense_H186R

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.