Variant (rsID / SNP)

rs16935065

rs16935065 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C8ORF34, C8orf34. Location: chromosome 8, position 69,699,756. The table records no clinical significance for this variant.

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Reference-table entries

C8ORF34Not classified

Variant type: missense_variant
Chromosome / position: 8:69699756
HGVS: NM_052958.4,c.1534G>A,p.Ala512Thr
Allele change: Missense_A495T

Associated conditions / phenotypes

Missense_A452T|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.