Variant (rsID / SNP)

rs1034405

rs1034405 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C3ORF18, C3orf18. Location: chromosome 3, position 50,597,092. The table records no clinical significance for this variant.

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Reference-table entries

C3ORF18Not classified

Variant type: missense_variant
Chromosome / position: 3:50597092
HGVS: NM_001171740.3,c.485C>T,p.Ala162Val
Allele change: Missense_A162V

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.