Variant (rsID / SNP)

rs17410000

rs17410000 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C5ORF22, C5orf22. Location: chromosome 5, position 31,538,692. The table records no clinical significance for this variant.

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Reference-table entries

C5ORF22Not classified

Variant type: missense_variant
Chromosome / position: 5:31538692
HGVS: NM_018356.3,c.703A>C,p.Thr235Pro
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.