Variant (rsID / SNP)

rs10783528

rs10783528 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT77. Location: chromosome 12, position 53,088,484. The table records no clinical significance for this variant.

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Reference-table entries

KRT77Not classified

Variant type: missense_variant
Chromosome / position: 12:53088484
HGVS: NM_175078.3,c.1006G>A,p.Asp336Asn
Allele change: Missense_D336N

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.