Variant (rsID / SNP)

rs10804166

rs10804166 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C2ORF80, C2orf80. Location: chromosome 2, position 209,036,712. The table records no clinical significance for this variant.

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Reference-table entries

C2ORF80Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 2:209036712
HGVS: NM_001099334.3,c.454A>G,p.Ser152Gly
Allele change: Missense_S152G

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.