Variant (rsID / SNP)

rs10777084

rs10777084 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C12ORF50, C12orf50. Location: chromosome 12, position 88,380,094. The table records no clinical significance for this variant.

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Reference-table entries

C12ORF50Not classified

Variant type: missense_variant
Chromosome / position: 12:88380094
HGVS: NM_152589.3,c.917A>G,p.Gln306Arg
Allele change: Missense_Q306R

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.