Variant (rsID / SNP)

rs358733

rs358733 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C3ORF33, C3orf33. Location: chromosome 3, position 155,485,302. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

C3ORF33Not classified

Variant type: missense_variant
Chromosome / position: 3:155485302
HGVS: NM_001308229.2,c.479G>A,p.Ser160Asn
Allele change: Missense_S160N

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.