Variant (rsID / SNP)

rs16859190

rs16859190 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C3ORF52, C3orf52. Location: chromosome 3, position 111,821,747. The table records no clinical significance for this variant.

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Reference-table entries

C3ORF52Not classified

Variant type: missense_variant
Chromosome / position: 3:111821747
HGVS: NM_001171747.2,c.331A>G,p.Ile111Val
Allele change: Missense_I111V

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.