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Variant (rsID / SNP)

rs2071461

CSNK2A3

rs2071461 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSNK2A3. Location: chromosome 11, position 11,373,960. The table records no clinical significance for this variant.

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Reference-table entries

CSNK2A3Not classified
Variant type
missense_variant
Chromosome / position
11:11373960
HGVS
NM_001256686.2,c.707G>A,p.Arg236His
Allele change
Silent

Public references

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