Variant (rsID / SNP)

rs13273355

rs13273355 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C8ORF48, C8orf48. Location: chromosome 8, position 13,424,583. The table records no clinical significance for this variant.

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Reference-table entries

C8ORF48Not classified

Variant type: missense_variant
Chromosome / position: 8:13424583
HGVS: NM_001007090.3,c.83C>T,p.Ser28Phe
Allele change: Silent

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.