Variant (rsID / SNP)

rs3803200

rs3803200 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C13ORF42, C13orf42. Location: chromosome 13, position 51,658,356. The table records no clinical significance for this variant.

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Reference-table entries

C13ORF42Not classified

Variant type: synonymous_variant
Chromosome / position: 13:51658356
HGVS: NM_001351589.3,c.909C>T,p.Tyr303Tyr
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.