Variant (rsID / SNP)

rs1567759

rs1567759 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT77. Location: chromosome 12, position 53,091,566. The table records no clinical significance for this variant.

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Reference-table entries

KRT77Not classified

Variant type: missense_variant
Chromosome / position: 12:53091566
HGVS: NM_175078.3,c.658G>T,p.Gly220Cys
Allele change: Missense_G220C

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.