Variant (rsID / SNP)

rs1258236

rs1258236 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C10ORF53, C10orf53. Location: chromosome 10, position 50,916,484. The table records no clinical significance for this variant.

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Reference-table entries

C10ORF53Not classified

Variant type: missense_variant
Chromosome / position: 10:50916484
HGVS: NM_182554.4,c.295A>G,p.Arg99Gly
Allele change: Missense_R99G

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.