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Variant (rsID / SNP)

rs2947594

C10ORF120C10orf120

rs2947594 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C10ORF120, C10orf120. Location: chromosome 10, position 124,457,452. The table records no clinical significance for this variant.

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Reference-table entries

C10ORF120Not classified
Variant type
missense_variant
Chromosome / position
10:124457452
HGVS
NM_001010912.4,c.805G>A,p.Ala269Thr
Allele change
Missense_A269T

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.